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The investigators will compare endobronchial ultrasound transbronchial needle aspiration (EBUS-TBNA) with intranodal forceps biopsy (EBUS-IFB) as it relates to the rate of diagnosis of suspected sarcoidosis.
This is prospective, single center randomized comparative study to determine the diagnostic yield and specimen quality of endobronchial ultrasound guided intranodal forceps biopsy of patients with suspected sarcoidosis based solely on imaging. This will be a single group study and will compare transbronchial needle aspiration via 19 or 21-gauge needle with intranodal forceps biopsy.
The study aims to answer a knowledge gap a as to whether the diagnostic yield and specimen quality of EBUS-TBNA with a 19G needle is less than those obtained by 1.9mm or greater intranodal forceps biopsy. The study proposed here will add to the field by further elucidating whether this procedure is beneficial for the diagnosis as it pertains to suspected sarcoidosis.
The anticipated required enrollment is 55 patients to achieve an α of 0.05 and β of 0.2. This assumes an unassisted diagnostic yield of 62.5% with standard of care EBUS-TBNA as reported in Ray et al, and a diagnostic supplementation to 80% yield with intranodal forceps biopsies.
References
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| EBUS-TBNA | Active Comparator | These will be the patient who undergo EBUS-TBNA only without EBUS-IFB |
|
| EBUS-TBNA + EBUS-IFB | Experimental | These will be the individuals who undergo EBUS-TBNA followed by EBUS-IFB in the same procedure |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Endobronchial Ultrasound-Guided Intranodal Forceps Biopsy | Procedure | Patients with mediastinal adenopathy will undergo EBUS-IFB and EBUS-TBNA during the same procedure to compare the yield of this procedure with EBUS-TBNA alone. |
| Measure | Description | Time Frame |
|---|---|---|
| Diagnostic Yield | Diagnostic yield of EBUS-TBNA + EBUS-IFB compared to EBUS-TBNA alone | 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| Duration of Procedure | Duration of combined EBUS-TBNA +IFB procedure compared to TBNA alone | 1 year |
| Complications | Complications of EBUS-TBNA +IFB procedure compared to TBNA alone |
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Inclusion Criteria:
Exclusion Criteria*:
These are the characteristics that a participant must NOT have in order to be eligible to participate in the study.
Order Number Criteria
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| Name | Affiliation | Role |
|---|---|---|
| Mardi Gomberg, MD | The George Washington University | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The George Washington University Hospital | Washington D.C. | District of Columbia | 20037 | United States |
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| ID | Term |
|---|---|
| D017565 | Sarcoidosis, Pulmonary |
| D008477 | Mediastinal Diseases |
| D012507 | Sarcoidosis |
| ID | Term |
|---|---|
| D017563 | Lung Diseases, Interstitial |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D008232 | Lymphoproliferative Disorders |
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1:1 randomization to EBUS-TBNA alone or EBUS-TBNA and EBUS-IFB
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The participant will be blinded to which group they were randomized to.
|
| 1 year |
| D008206 | Lymphatic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D006968 | Hypersensitivity, Delayed |
| D006967 | Hypersensitivity |
| D007154 | Immune System Diseases |
| D013896 | Thoracic Diseases |