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This study is being conducted this study to determine whether injections of Xeomin®, a type of botulinum toxin into the glands that produce saliva (one pair just below and in front of the ear and the other just under the jaw line) are safe and effective to treat excessive saliva, or drooling in patients with Parkinson's Disease (PD)/parkinsonism.
Participants will be recruited if they have Parkinson's disease, Parkinsonism. Inclusion and exclusion criteria are summarized below. Participants will be screened at the first visit to make sure they are eligible for the trial. They will then undergo baseline testing including neurologic evaluation, questions to assess their memory and cognitive status and evaluation of their disease status using parts of the Unified Parkinsons's Disease Ratings Scale (UPDRS) that are routinely used to follow disease progression. They will be given a questionnaire to evaluate the severity of their drooling. Their saliva production will be measured by having them spit into a cup for 5 minutes, twice.
At the first visit, after making sure they are eligible for the study and performing the baseline testing and procedures, they will be given either Xeomin or placebo (saline injections without medication) injections in the 4 glands that produce saliva. They will not know which injection they received. This visit will take about 2 hours. They will be followed up every month and asked about side effects, have neurologic evaluation and UPDRS testing and fill-in the questionnaire for drooling severity. Saliva volume will be measured as done at the first visit. At either Month 4 or 5, participants will receive the second injection. This will be a "cross-over" injection, i.e., if they received Xeomin at the first injection they will receive saline at the second and vice versa. Thus, all participants will receive the study medication Xeomin, either as the first injection or the second injection at 4 months or 5 months. The follow up after the second injection will be one monthly visit for 3 months, with similar evaluations as described above. The follow-up visit will take about 1 hour each.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Incobotulinum Toxin A | Experimental | Twenty units (0.2 ml) of incobotulinum toxin A injected into each parotid gland and 30 units (0.3 ml) to each submandibular gland for a total dose of 100 units using anatomical landmarks |
|
| Placebo | Placebo Comparator | Sterile, preservative free 0.9% saline, 1 ml, was used as placebo, and injected into the parotid (0.2 ml each) and submandibular (0.3ml each) glands . |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Incobotulinum Toxin A | Drug | Twenty units (0.2 ml) of incobotulinum toxin A were injected into each parotid gland and 30 units (0.3 ml) to each submandibular gland for a total dose of 100 units using anatomical landmarks |
| Measure | Description | Time Frame |
|---|---|---|
| Objectively Measured Salivary Weight | Change in saliva weight between baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period. | baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period |
| Objectively Measured Percentage Salivary Weight | Percentage change in saliva weight between baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period. | baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Drooling Frequency and Severity Scale (DFSS) Scores | measured between baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period.Drooling Frequency and Severity Score. The Drooling Score equals the sum of the Severity and Frequency sub-scores. The range is 2-9, higher numbers represent worse drooling Drooling Severity Scale
1. = No drooling 2. = Occasionally drools 3. = Frequently drools 4. = Constant drooling |
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Inclusion Criteria:
For PD/ Parkinsonism: 1. PD, Multiple Systems Atrophy (MSA), or Progressive Supranuclear Palsy (PSP) diagnosed by clinical criteria, ages 20-80 with troublesome sialorrhea as defined below**.
Sialorrhea that patients or their families or treating physicians think is troublesome
Exclusion Criteria:
For PD:
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| Name | Affiliation | Role |
|---|---|---|
| Pushpa Narayanaswami, MD | Beth Israel Deaconess Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Beth Israel Deaconess Medical Center | Boston | Massachusetts | 02215 | United States |
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17 subjects were assessed; 7 were excluded because they did not meet study criteria. This was a cross over study; all subjects received both placebo and Incobotulinum toxin injections and were followed up for 3 months after each injection. Washout period was 1-2 months, saliva weight had to be ≥ (baseline- 0.5 SD), to receive the second injection
Subjects with Parkinson's disease/ parkinsonism with troublesome sialorrhea were recruited from the Movement Disorders clinic at Beth Israel Deaconess Medical Center, Boston, and by providing information to neurologists around the Boston area. Ten subjects were recruited between 9/5/2012 and 2/26/2014. The last study visit was completed on 9/5/14
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| ID | Title | Description |
|---|---|---|
| FG000 | Placebo First, Then Incobotulinum Toxin A | sterile, preservative free 0.9% saline, 1 ml of saline into the parotid and submandibular glands in first intervention period |
| FG001 | Incobotulinum Toxin A First, Then Placebo | Incobotulinum toxin, 100 units, diluted in 1 ml 0.9% sterile saline. 20 units (0.2 ml) were injected into each parotid gland and 30 units (0.3 ml) into each submandibular gland using anatomical landmarks |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| First Intervention |
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| Washout 1-2 Months |
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| Second Intervention |
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Ten subjects were recruited; nine completed both periods of the study. One subject dropped out after the first injection because he wanted to start anticholinergics for symptomatic treatment of tremor, and this was an exclusion criterion. His data was excluded.
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| ID | Title | Description |
|---|---|---|
| BG000 | All Study Participants | Participants who received either Placebo, 1ml of preservative free sterile 0.9% saline, injected into the parotid (0.2 ml each) and submandibular ( 0.3 ml each), or Incobotulinum Toxin A 100 units, 20 units (0.2 ml) of Inco-A were injected into each parotid gland and 30 units (0.3 ml) to each submandibular gland using anatomical landmarks |
| Units | Counts |
|---|---|
| Participants |
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| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | 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 | Objectively Measured Salivary Weight | Change in saliva weight between baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period. | Posted | Mean | Standard Deviation | gm | baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period |
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Adverse events data were collected for each subject at monthly visits for the duration of the study, 7-8 months per subject
all subjects were asked at each monthly visit if they had experienced any adverse events since the previous visit. If they responded yes, a checklist of common and rare side effects was used to query subjects, their adverse events were recorded in a standardized fashion and reported to the Committee for Clinical Investigations as per regulations
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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 | Incobotulinum Toxin | Incobotulinum Toxin 100 units diluted in 1 ml of sterile 0.9% saline injected in the parotid (20 units, 0.2 ml each) and submandibular (30 units, 0.3ml each) glands of subjects |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| chewing difficulty | Gastrointestinal disorders | Non-systematic Assessment | difficulty in chewing, a sensation of swelling inside the cheeks, a tendency to bite the inside of her cheeks and difficulty with motor control of the tongue, mild, resolved in 4-6 weeks without intervention |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr. Pushpa Narayanaswami | Beth Israel Deaconess Medical center | 617-667-8130 | pnarayan@bidmc.harvard.edu |
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| ID | Term |
|---|---|
| D012798 | Sialorrhea |
| ID | Term |
|---|---|
| D012466 | Salivary Gland Diseases |
| D009059 | Mouth Diseases |
| D009057 | Stomatognathic Diseases |
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| ID | Term |
|---|---|
| C545476 | incobotulinumtoxinA |
| D012965 | Sodium Chloride |
| ID | Term |
|---|---|
| D002712 | Chlorides |
| D006851 | Hydrochloric Acid |
| D017606 | Chlorine Compounds |
| D007287 | Inorganic Chemicals |
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| Placebo | Drug | Sterile, preservative free 0.9% saline, 1 ml, was used as placebo, and injected into the parotid (0.2 ml each) and submandibular (0.3ml each) glands . |
|
|
| baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period |
| Number of Participants With Response, Defined as Subjects With ≥ 2 Point Improvement in the DFSS Scores. | measured between baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period. | baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period |
| Number of Participants With Response, Defined as Subjects With ≥ 20% Reduction in Saliva Volume. | measured between baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period | between baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period |
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| years |
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| Sex: Female, Male | Count of Participants | Participants |
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| Region of Enrollment | Number | participants |
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| UPDRS | Unified Parkinsons Disease Rating Scale. The UPDRS is a rating tool to follow the longitudinal course of Parkinson's Disease. It is made up of the 1) Mentation, Behavior, and Mood, 2) Activities of Daily Living and 3) Motor sections. These are evaluated by interview. We used UPDRS, Part 2 Questions 5,6,7 evaluating speech, salivation and swallowing and Part 3 questions 18 and 19 for motor examination of speech and facial expression. The scores for these sections were summed to obtain the total score. The range possible is 0- 20, with 20 reflecting worse disability | Median | Inter-Quartile Range | units on a scale |
|
| DFSS | Drooling Frequency and Severity Score: The Drooling Score equals the sum of the Severity and Frequency sub-scores.The total score ranges from 2 to 9, with higher scores indicating more severe and frequent drooling Drooling Severity Scale
Drooling Frequency Scale
| Median | Inter-Quartile Range | units on a scale |
|
| saliva weight | Mean | Standard Deviation | gms |
|
|
|
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| Primary | Objectively Measured Percentage Salivary Weight | Percentage change in saliva weight between baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period. | Posted | Mean | Standard Deviation | percentage change from baseline | baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period |
|
|
|
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| Secondary | Change in Drooling Frequency and Severity Scale (DFSS) Scores | measured between baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period.Drooling Frequency and Severity Score. The Drooling Score equals the sum of the Severity and Frequency sub-scores. The range is 2-9, higher numbers represent worse drooling Drooling Severity Scale
1. = No drooling 2. = Occasionally drools 3. = Frequently drools 4. = Constant drooling | Posted | Mean | Standard Deviation | units on a scale | baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period |
|
|
|
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| Secondary | Number of Participants With Response, Defined as Subjects With ≥ 2 Point Improvement in the DFSS Scores. | measured between baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period. | Posted | Number | participants | baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period |
|
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| Secondary | Number of Participants With Response, Defined as Subjects With ≥ 20% Reduction in Saliva Volume. | measured between baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period | Posted | Number | participants | between baseline and one month post-injection in the Incobotulinum toxin A period compared to the placebo period |
|
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| 0 |
| 9 |
| 2 |
| 9 |
| EG001 | Placebo | Sterile, preservative free 0.9% saline, 1 mL injected into the parotid (0.2 ml each) and submandibular (0.3ml each) glands . | 0 | 10 | 0 | 9 |
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| viscous saliva | Gastrointestinal disorders | Non-systematic Assessment | viscous, thick saliva, mild, resolved in 4-6 weeks without intervention |
|
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| D017670 |
| Sodium Compounds |