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Percutaneous Interruption of the Coracohumeral Ligament for the treatment of Frozen Shoulder.
Chronic inflammation of the shoulder joint capsule and its associated structures can lead to clinically significant symptoms, including insidious onset of pain, and ultimately restricting range of motion. Although the underlying mechanism for adhesive capsulitis (AC) is not well defined, some studies suggest that fibroblast proliferation and thickening of the coracohumeral ligament (CHL) is a proposed mechanism for which AC and subsequent prolonged immobilization and symptoms present (1, 2, 3). Other studies suggest that it is due to a combination of capsular fibrosis and inflammation within the synovium, and other focus on the fact that thickening of the CHL is responsible for limiting external rotation in patients affected by adhesive capsulitis (1).
AC coined frozen shoulder by Codman in 1934 [2), has an estimated prevalence of 2-3% in the general population, with ages 40-70 affected most commonly, and predominantly women. While the precise etiology remains undefined, it can be secondary to trauma or an idiopathic etiology and has been found to have an incidence as high as 20% in diabetic patients, with worse functional outcomes when compared to non-diabetic patients. Hypothyroidism and cerebrovascular disease have also been shown to be associated with an increased risk of developing AC (4). AC is typically a clinical diagnosis. However, both magnetic resonance and ultrasonography have consistently shown thickening of the CHL (1). Several studies have compared arthrographic evidence of findings in adhesive capsulitis, and many reported a thickening of the CHL in cases of frozen shoulder as compared to control subjects (2). In a study implementing shear-wave elastography (SWE), the CHL in patients diagnosed with adhesive capsulitis was thicker and stiffer (4).
Interventions aimed at improving AC and CHL damage, clinical symptomatology, as well as histopathological findings range from rest and physical therapy, local injections and hydrodilation, to advanced surgical interventions (4, 5). These surgical options include manipulation under anesthesia (MUA) and arthroscopic capsulotomy. MUA is an aggressive mobilization of the joint in an effort to lyse adhesions and to stretch the contracted glenohumeral capsule. Despite potential benefits, MUA has been associated with superior labral anterior and posterior (SLAP) lesions, bankart lesions, capsular tears, hemarthrosis, and even humeral or glenoid fractures (4). Arthroscopic capsulotomy allows for direct visualization of the CHL and confirmation of the diagnosis of AC, and several studies have shown improvement in pain relief as well as range of motion (4). However, patients who did not benefit from this intervention were women, typically over the age of 50, with a past medical history of diabetes mellitus. CHL resection has also been described as a potential treatment option for AC (6, 7), with current therapy limited to a surgical approach. Management of refractory disease through arthroscopic capsular release has been shown to improve pain and increase range-of-motion (8, 9, 4). A sequela of arthroscopic surgery is postoperative persistent AC, which some surgeons attempt to prophylactically prevent with adequate postoperative pain control so that the patient can participate in a physical therapy program. The potential limitations of current conservative management and IRB NUMBER: 2020-11998 IRB APPROVAL DATE: 11/17/2020 sequelae of surgical approaches have prompted additional novel therapies. International have researchers developed an ultrasound guided technique with a scalpel incision of the CHL to address this need. Scalpel use is not the standard of care for interventional musculoskeletal pain treatments and our team decided to improve this limitation. Blades and scalpels limit US visibility, thus marginalizing the safety of the procedure. Our team used a percutaneous, ultrasound visible, needle shaped, tissue cutting device to lesion the CHL while improving upon the potential safety concerns. The tool, TENEX®, is widely used by Pain physicians to perform percutaneous tenotomies and has been described in the management of various tendinous pathologies (10, 11, 12, 13, 14, 15).; this device was selected because the gross architectural similarities of tendon and ligament suggest that the CHL could be modified by this tool. Our novel procedure was performed on cadavers to provide proof of concept
The authors performed cadaveric dissection in 8 cadaveric shoulders with the hypothesis that sonographically guided percutaneous dissection will result in sectioning of the coracohumeral ligament. In this study we found that complete sectioning was reproducibly achieved in 7 minutes with approximately 250 passes of the device. This was the desired outcome for improving the shoulder ROM (16). This shows proof of concept and we want to perform this procedure in living subjects for validation. If the results are positive patients can have an outpatient procedure in the interventional pain clinic with desirable results. This cadaveric technique study has already been submitted to Pain Medicine journal for publication.
In addition to the above proof of concept above this procedure was performed in living subjects. A peer reviewed paper was submitted based on data from these subjects. 7 patients were selected for the publication as these patients had follow-ups as requested by the reviewer. In these patients the average improvement in external rotation was 40 degrees and the average abduction improvement was 31 degrees. All patients retained this improvement in shoulder ROM at follow-up visits. Of note, one patients follow-up visit was 116 after the procedure and her improvement in ROM was 60 and 110 in external rotation and abduction respectively. Given these outcomes the authors decided to do a prospective RCT.](streamdown:incomplete-link)
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Tenex plus local anesthetic | Experimental | Use of the TENEX device for sectioning of the CHL |
|
| Local Anesthetic | Other | Only Local anesthetic will be injected into the CHL. This arm will have the option to cross over into Tenex arm at 1 month |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Tenex | Device | Local anesthetic plus Tenex into the coracohumeral ligament for adhesive capsulitis |
|
| Measure | Description | Time Frame |
|---|---|---|
| Comparison of Range of Motion of the Shoulder | Change in shoulder range of motion (ROM) (external rotation and abduction) procedure by at least 100%, measured with goniometer. Increased degrees of motion is indicative of more favorable/better outcomes. | Immediately following procedure, up to 60 minutes |
| Measure | Description | Time Frame |
|---|---|---|
| Durability of Local Anesthetic - Change in Range Of Motion (ROM) | Shoulder abduction and external rotation measured with goniometer. Increased degrees of motion is indicative of more favorable/better outcomes. | Baseline (Before the procedure) and at 1 month |
| Durability of the TENEX - Change in Range Of Motion (ROM) |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Sayed Wahezi, MD | Montefiore Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Montefiore Medical Center | New York | New York | 10461 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 26323030 | Background | Wu CH, Chen WS, Wang TG. Elasticity of the Coracohumeral Ligament in Patients with Adhesive Capsulitis of the Shoulder. Radiology. 2016 Feb;278(2):458-64. doi: 10.1148/radiol.2015150888. Epub 2015 Aug 31. | |
| 15358849 | Background | Mengiardi B, Pfirrmann CW, Gerber C, Hodler J, Zanetti M. Frozen shoulder: MR arthrographic findings. Radiology. 2004 Nov;233(2):486-92. doi: 10.1148/radiol.2332031219. Epub 2004 Sep 9. |
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| ID | Title | Description |
|---|---|---|
| FG000 | Local Anesthetic First Then Tenex Plus Local Anesthetic | Local anesthetic injected into the CHL. Patients in this arm also had the option to cross over into Tenex plus Local Anesthetic arm at 1 month (~4 weeks). Procedure Description: Local anesthetic: Local anesthetic into the coracohumeral ligament for adhesive capsulitis Tenex: Local anesthetic plus Tenex into the coracohumeral ligament for adhesive capsulitis |
| FG001 | Tenex Plus Local Anesthetic Alone | Use of the TENEX device for sectioning of the CHL Procedure Description: Tenex: Local anesthetic plus Tenex into the coracohumeral ligament for adhesive capsulitis Local anesthetic: Local anesthetic into the coracohumeral ligament for adhesive capsulitis |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| First Intervention (4 Weeks) |
| |||||||||||||
| Optional Second Intervention (11 Months) |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Tenex Plus Local Anesthetic Alone | Use of the TENEX device for sectioning of the CHL Procedure Description: Tenex: Local anesthetic plus Tenex into the coracohumeral ligament for adhesive capsulitis Local anesthetic: Local anesthetic into the coracohumeral ligament for adhesive capsulitis |
| BG001 |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Customized | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Comparison of Range of Motion of the Shoulder | Change in shoulder range of motion (ROM) (external rotation and abduction) procedure by at least 100%, measured with goniometer. Increased degrees of motion is indicative of more favorable/better outcomes. | Posted | Mean | Standard Deviation | degrees | Immediately following procedure, up to 60 minutes |
|
Each patient was followed for adverse events from the date of enrollment into the study until the date of their last follow-up, approximately 1 year.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Tenex Plus Local Anesthetic Alone | Use of the TENEX device for sectioning of the CHL There were 30 subjects directly enrolled to TENEX group and 1 out of these 30 subjects had SAE. After 9 Subjects' crossing over, there were totally 39 subject who got the TENEX procedure in this group. 3 out of 9 crossed over subjects had SAE after crossing over. So, totally 4 subjects had SAE after receiving the TENEX procedure. Procedure Description: Tenex: Local anesthetic plus Tenex into the coracohumeral ligament for adhesive capsulitis Local anesthetic: Only local anesthetic into the coracohumeral ligament for adhesive capsulitis |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Serious Adverse Event | Surgical and medical procedures | Non-systematic Assessment | Subject underwent the reverse shoulder arthroplasty on the effected (study) site |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Shoulder Trauma | Musculoskeletal and connective tissue disorders | Non-systematic Assessment | Shoulder trauma which was not related to study procedures |
This study represents a small population of patients with a CHL-related ROM deficit.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Sayed Wahezi, M.D. | Albert Einstein College of Medicine | 718-920-7246 | swahezi@montefiore.org |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP_ICF | Yes | Yes | Yes | Study Protocol, Statistical Analysis Plan, and Informed Consent Form | Feb 13, 2024 | Feb 14, 2024 | Prot_SAP_ICF_000.pdf |
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| ID | Term |
|---|---|
| D002062 | Bursitis |
| ID | Term |
|---|---|
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
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| ID | Term |
|---|---|
| D000779 | Anesthetics, Local |
| ID | Term |
|---|---|
| D000777 | Anesthetics |
| D002492 | Central Nervous System Depressants |
| D045505 | Physiological Effects of Drugs |
| D020228 | Pharmacologic Actions |
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| Local anesthetic | Drug | Only local anesthetic into the coracohumeral ligament for adhesive capsulitis |
|
Shoulder abduction and external rotation measured with goniometer. Increased degrees of motion is indicative of more favorable/better outcomes. |
| Immediately after the procedure and at the long term follow-up (10 months to 2 years) |
| Change of Pain Intensity Score for Local Anesthetic Group | Measured by visual analog scale (VAS). VAS is a validated, subjective measure for for acute and chronic pain. Range of possible values: 0-10. (Higher score indicates more pain) | at the Baseline visit (Before the procedure) and at the 1-month visit |
| Change of Pain Intensity Score for TENEX Group | Measured by visual analog scale (VAS). VAS is a validated, subjective measure for for acute and chronic pain. Range of possible values: 0-10. (Higher score indicates more pain) | at the Baseline visit (before the procedure) and at the long-term follow-up (10 months to 2 years) |
| Change of the Oxford Shoulder Score for Local Anesthetic Group | Measured by The Oxford Shoulder Score (OSS) questionnaire form. The Oxford Shoulder Score (OSS) is a 12-item patient-report questionnaire with a 0-4 scoring format, developed to identify functional changes of the shoulder. Range of possible values: 0-48. (Higher score represents a better outcome) | at the baseline (before the procedure) and at the 1-month visit |
| Change of the Oxford Shoulder Score for TENEX Group | Measured by The Oxford Shoulder Score (OSS) questionnaire form. The Oxford Shoulder Score (OSS) is a 12-item patient-report questionnaire with a 0-4 scoring format, developed to identify functional changes of the shoulder. Range of possible values: 0-48. (Higher score represents a better outcome) | at the baseline (before the procedure) and at the long term follow-up (10 months to 2 years) |
| 16356983 | Background | Dias R, Cutts S, Massoud S. Frozen shoulder. BMJ. 2005 Dec 17;331(7530):1453-6. doi: 10.1136/bmj.331.7530.1453. |
| 28405218 | Background | Le HV, Lee SJ, Nazarian A, Rodriguez EK. Adhesive capsulitis of the shoulder: review of pathophysiology and current clinical treatments. Shoulder Elbow. 2017 Apr;9(2):75-84. doi: 10.1177/1758573216676786. Epub 2016 Nov 7. |
| 22405512 | Background | Maund E, Craig D, Suekarran S, Neilson A, Wright K, Brealey S, Dennis L, Goodchild L, Hanchard N, Rangan A, Richardson G, Robertson J, McDaid C. Management of frozen shoulder: a systematic review and cost-effectiveness analysis. Health Technol Assess. 2012;16(11):1-264. doi: 10.3310/hta16110. |
| 30288192 | Background | Hagiwara Y, Sekiguchi T, Ando A, Kanazawa K, Koide M, Hamada J, Yabe Y, Yoshida S, Itoi E. Effects of Arthroscopic Coracohumeral Ligament Release on Range of Motion for Patients with Frozen Shoulder. Open Orthop J. 2018 Sep 18;12:373-379. doi: 10.2174/1874325001812010373. eCollection 2018. |
| 29567320 | Background | Yukata K, Goto T, Sakai T, Fujii H, Hamawaki J, Yasui N. Ultrasound-guided coracohumeral ligament release. Orthop Traumatol Surg Res. 2018 Oct;104(6):823-827. doi: 10.1016/j.otsr.2018.01.016. Epub 2018 Mar 19. |
| 17519989 | Background | Austgulen OK, Oyen J, Hegna J, Solheim E. [Arthroscopic capsular release in treatment of primary frozen shoulder]. Tidsskr Nor Laegeforen. 2007 May 17;127(10):1356-8. Norwegian. |
| 12355929 | Background | Chen SK, Chien SH, Fu YC, Huang PJ, Chou PH. Idiopathic frozen shoulder treated by arthroscopic brisement. Kaohsiung J Med Sci. 2002 Jun;18(6):289-94. |
| 28842108 | Background | Sanchez PJ, Grady JF, Saxena A. Percutaneous Ultrasonic Tenotomy for Achilles Tendinopathy Is a Surgical Procedure With Similar Complications. J Foot Ankle Surg. 2017 Sep-Oct;56(5):982-984. doi: 10.1053/j.jfas.2017.06.015. |
| 25986341 | Background | Kamineni S, Butterfield T, Sinai A. Percutaneous ultrasonic debridement of tendinopathy-a pilot Achilles rabbit model. J Orthop Surg Res. 2015 May 20;10:70. doi: 10.1186/s13018-015-0207-7. |
| 30280399 | Background | Chimenti RL, Stover DW, Fick BS, Hall MM. Percutaneous Ultrasonic Tenotomy Reduces Insertional Achilles Tendinopathy Pain With High Patient Satisfaction and a Low Complication Rate. J Ultrasound Med. 2019 Jun;38(6):1629-1635. doi: 10.1002/jum.14835. Epub 2018 Oct 2. |
| 25306494 | Background | Barnes DE, Beckley JM, Smith J. Percutaneous ultrasonic tenotomy for chronic elbow tendinosis: a prospective study. J Shoulder Elbow Surg. 2015 Jan;24(1):67-73. doi: 10.1016/j.jse.2014.07.017. Epub 2014 Oct 8. |
| 23302261 | Background | Koh JS, Mohan PC, Howe TS, Lee BP, Chia SL, Yang Z, Morrey BF. Fasciotomy and surgical tenotomy for recalcitrant lateral elbow tendinopathy: early clinical experience with a novel device for minimally invasive percutaneous microresection. Am J Sports Med. 2013 Mar;41(3):636-44. doi: 10.1177/0363546512470625. Epub 2013 Jan 9. |
| 18791678 | Background | Zhu J, Hu B, Xing C, Li J. Ultrasound-guided, minimally invasive, percutaneous needle puncture treatment for tennis elbow. Adv Ther. 2008 Oct;25(10):1031-6. doi: 10.1007/s12325-008-0099-6. |
| 16724200 | Background | Homsi C, Bordalo-Rodrigues M, da Silva JJ, Stump XM. Ultrasound in adhesive capsulitis of the shoulder: is assessment of the coracohumeral ligament a valuable diagnostic tool? Skeletal Radiol. 2006 Sep;35(9):673-8. doi: 10.1007/s00256-006-0136-y. Epub 2006 May 25. |
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| Local Anesthetic First Then Tenex Plus Local Anesthetic |
Only Local anesthetic injected into the CHL. Patients in this arm had the option to cross over into Tenex plus Local Anesthetic arm at 1 month (~4 weeks). Procedure Description: Local anesthetic: Local anesthetic into the coracohumeral ligament for adhesive capsulitis Tenex: Local anesthetic plus Tenex into the coracohumeral ligament for adhesive capsulitis |
| BG002 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
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| Race and Ethnicity Not Collected | Race and Ethnicity were not collected from any participant. | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| BMI | Mean | Standard Deviation | kg/m^2 |
|
| Affected Arm (Right/Left) | The affected arm (Ieft or right) of each patient is noted. | Number | participants |
|
Only Local anesthetic injected into the CHL. Patients in this arm had the option to cross over into Tenex plus Local Anesthetic arm at 1 month (~4 weeks).
Procedure Description:
Local anesthetic: Local anesthetic into the coracohumeral ligament for adhesive capsulitis
Tenex: Local anesthetic plus Tenex into the coracohumeral ligament for adhesive capsulitis
|
|
| Secondary | Durability of Local Anesthetic - Change in Range Of Motion (ROM) | Shoulder abduction and external rotation measured with goniometer. Increased degrees of motion is indicative of more favorable/better outcomes. | Posted | Mean | Standard Deviation | degrees | Baseline (Before the procedure) and at 1 month |
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| Secondary | Durability of the TENEX - Change in Range Of Motion (ROM) | Shoulder abduction and external rotation measured with goniometer. Increased degrees of motion is indicative of more favorable/better outcomes. | In addition to 26 subjects in the TENEX group, 9 Subjects in Control group were crossed over into the TENEX arm at their 1-month visit. | Posted | Mean | Standard Deviation | degrees | Immediately after the procedure and at the long term follow-up (10 months to 2 years) |
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| Secondary | Change of Pain Intensity Score for Local Anesthetic Group | Measured by visual analog scale (VAS). VAS is a validated, subjective measure for for acute and chronic pain. Range of possible values: 0-10. (Higher score indicates more pain) | Posted | Median | Inter-Quartile Range | score on a scale | at the Baseline visit (Before the procedure) and at the 1-month visit |
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| Secondary | Change of Pain Intensity Score for TENEX Group | Measured by visual analog scale (VAS). VAS is a validated, subjective measure for for acute and chronic pain. Range of possible values: 0-10. (Higher score indicates more pain) | In addition to 26 subjects in the TENEX group, 9 Subjects in Control group were crossed over into the TENEX arm at their 1-month visit. | Posted | Median | Inter-Quartile Range | score on a scale | at the Baseline visit (before the procedure) and at the long-term follow-up (10 months to 2 years) |
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| Secondary | Change of the Oxford Shoulder Score for Local Anesthetic Group | Measured by The Oxford Shoulder Score (OSS) questionnaire form. The Oxford Shoulder Score (OSS) is a 12-item patient-report questionnaire with a 0-4 scoring format, developed to identify functional changes of the shoulder. Range of possible values: 0-48. (Higher score represents a better outcome) | Posted | Mean | Standard Deviation | score on a scale | at the baseline (before the procedure) and at the 1-month visit |
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| Secondary | Change of the Oxford Shoulder Score for TENEX Group | Measured by The Oxford Shoulder Score (OSS) questionnaire form. The Oxford Shoulder Score (OSS) is a 12-item patient-report questionnaire with a 0-4 scoring format, developed to identify functional changes of the shoulder. Range of possible values: 0-48. (Higher score represents a better outcome) | In addition to 26 subjects in the TENEX group, 9 Subjects in Control group were crossed over into the TENEX arm at their 1-month visit. | Posted | Mean | Standard Deviation | score on a scale | at the baseline (before the procedure) and at the long term follow-up (10 months to 2 years) |
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| 0 |
| 30 |
| 4 |
| 30 |
| 1 |
| 30 |
| EG001 | Local Anesthetic First Then Tenex Plus Local Anesthetic | Only Local anesthetic injected into the CHL. This arm had the option to cross over into Tenex arm at 1 month. There were 16 subjects enrolled to Local Anesthetic group. 9 Subjects crossed over into TENEX group at the one month follow-up. So after 1 month follow-up, Only 7 Subjects remained in Local Anesthetic group and these 7 subjects did not have any SAE. 3 out of 9 crossed over subjects had SAE after crossing over. Procedure Description: Local anesthetic: Only local anesthetic into the coracohumeral ligament for adhesive capsulitis | 0 | 16 | 0 | 16 | 0 | 16 |
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| D020164 | Chemical Actions and Uses |
| D018689 | Sensory System Agents |
| D018373 | Peripheral Nervous System Agents |
| D002491 | Central Nervous System Agents |
| D045506 | Therapeutic Uses |
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| Abduction at 1-Month |
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| Abduction in the long term |
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