An RCT of NBI vs. White Light Guided Endobronchial Biopsy in Suspected Sarcoidosis (NABS)
Primary Purpose
Sarcoidosis, Pulmonary
Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Narrow band imaging bronchoscopy guided endobronchial biopsy
White light bronchscopy guided endobronchial biopsy
Sponsored by
About this trial
This is an interventional diagnostic trial for Sarcoidosis, Pulmonary
Eligibility Criteria
Inclusion Criteria:
- Age more than 18 years.
- Clinical presentation and radiological findings (enlarged hilar and or mediastinal lymph nodes >10 mm [short axis], and/or perilymphatic nodules or peribronchovascular thickening on computed tomography [CT] chest) suggesting sarcoidosis.
- Willing to give informed consent.
Exclusion Criteria:
- Hemodynamic instability (systolic BP <100 mm Hg).
- Pregnancy.
- Treatment with systemic glucocorticoids for more than three weeks in the preceding three months.
- Diagnosis of sarcoidosis possible with another minimally invasive technique such as skin biopsy or peripheral lymph node biopsy.
Sites / Locations
- Postgraduate Institute of Medical Education and Research
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Narrow band imaging bronchoscopy
White light bronchoscopy
Arm Description
The narrow band imaging mode uses two narrow bands of light with wavelengths of 390-445 nm and 530-550 nm.
The white light bronchoscopy mode uses the entire range of white light wavelengths, 400-700 nm.
Outcomes
Primary Outcome Measures
Yield of granulomatous inflammation in endobronchial biopsy in subjects with a final diagnosis of sarcoidosis
Diagnostic yield of endobronchial biopsy (demonstration of granulomatous inflammation in EBB specimen, in subjects with a final diagnosis of sarcoidosis)
Secondary Outcome Measures
Complications: Bleeding
The incidence of bleeding after the endobronchial biopsy
Procedure duration
Duration of procedure (from the time of entry into the trachea till the completion of the endobronchial biopsy)
Full Information
NCT ID
NCT05311150
First Posted
March 26, 2022
Last Updated
March 28, 2023
Sponsor
Postgraduate Institute of Medical Education and Research
1. Study Identification
Unique Protocol Identification Number
NCT05311150
Brief Title
An RCT of NBI vs. White Light Guided Endobronchial Biopsy in Suspected Sarcoidosis
Acronym
NABS
Official Title
A Randomized Control Trial to Compare the Diagnostic Yield of Endobronchial Biopsy Performed Under Direct Narrow Band Imaging or White Light Bronchoscopy Guidance in Suspected Sarcoidosis
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
January 1, 2022 (Actual)
Primary Completion Date
January 31, 2023 (Actual)
Study Completion Date
February 15, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Postgraduate Institute of Medical Education and Research
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
In the diagnosis of patients with sarcoidosis, there is paucity of literature on the diagnostic yield of the endobronchial biopsies obtained with narrow band imaging (NBI) bronchoscopy. The present study aims to compare the diagnostic yield of endobronchial biopsyperformed under direct narrow band imaging or white light bronchoscopy guidance in suspected sarcoidosis.We hypothesize that the use of NBI will improve the yield of endobronchial biopsy in patients with sarcoidosis.
Detailed Description
The present study will be a randomized controlled trial. It will be performed in the Bronchoscopy suite of the Department of Pulmonary Medicine, PGIMER. Subjects meeting the selection criteria will be randomized 1:1 to undergo EBB under real-time visualization with NBI or white light bronchoscopy. The randomization sequence will be computer generated and the study group allocations will be placed in opaque sealed envelopes. They will be opened just before the performance of the bronchoscopic procedures.
Primary outcome:the diagnostic yield of EBB (demonstration of granulomatous inflammation in EBB specimen, in subjects with a final diagnosis of sarcoidosis)
Secondary outcomes:
Complications related to the procedure (bleeding)
Duration of procedure (from the time of entry into the trachea till the completion of the endobronchial biopsy)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sarcoidosis, Pulmonary
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
The pathologist analyzing the biopsy specimen will be masked.
Allocation
Randomized
Enrollment
150 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Narrow band imaging bronchoscopy
Arm Type
Active Comparator
Arm Description
The narrow band imaging mode uses two narrow bands of light with wavelengths of 390-445 nm and 530-550 nm.
Arm Title
White light bronchoscopy
Arm Type
Active Comparator
Arm Description
The white light bronchoscopy mode uses the entire range of white light wavelengths, 400-700 nm.
Intervention Type
Device
Intervention Name(s)
Narrow band imaging bronchoscopy guided endobronchial biopsy
Intervention Description
Examination of the airways will be performed with the narrow band imaging mode using a flexible video-bronchoscope (BF-1T 180, Olympus Medical, Japan). Endobronchial biopsies will be performed from the abnormal areas as deemed by the operator.
Intervention Type
Device
Intervention Name(s)
White light bronchscopy guided endobronchial biopsy
Intervention Description
Examination of the airways will be performed with the white light bronchoscopy mode using a flexible video-bronchoscope (BF-1T 180, Olympus Medical, Japan). Endobronchial biopsies will be performed from the abnormal areas as deemed by the operator.
Primary Outcome Measure Information:
Title
Yield of granulomatous inflammation in endobronchial biopsy in subjects with a final diagnosis of sarcoidosis
Description
Diagnostic yield of endobronchial biopsy (demonstration of granulomatous inflammation in EBB specimen, in subjects with a final diagnosis of sarcoidosis)
Time Frame
7 days
Secondary Outcome Measure Information:
Title
Complications: Bleeding
Description
The incidence of bleeding after the endobronchial biopsy
Time Frame
1 day
Title
Procedure duration
Description
Duration of procedure (from the time of entry into the trachea till the completion of the endobronchial biopsy)
Time Frame
1 day
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age more than 18 years.
Clinical presentation and radiological findings (enlarged hilar and or mediastinal lymph nodes >10 mm [short axis], and/or perilymphatic nodules or peribronchovascular thickening on computed tomography [CT] chest) suggesting sarcoidosis.
Willing to give informed consent.
Exclusion Criteria:
Hemodynamic instability (systolic BP <100 mm Hg).
Pregnancy.
Treatment with systemic glucocorticoids for more than three weeks in the preceding three months.
Diagnosis of sarcoidosis possible with another minimally invasive technique such as skin biopsy or peripheral lymph node biopsy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ashutosh N Aggarwal, MD, DM
Organizational Affiliation
PGIMER, Chandigarh, India
Official's Role
Study Chair
Facility Information:
Facility Name
Postgraduate Institute of Medical Education and Research
City
Chandigarh
ZIP/Postal Code
160012
Country
India
12. IPD Sharing Statement
Plan to Share IPD
No
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An RCT of NBI vs. White Light Guided Endobronchial Biopsy in Suspected Sarcoidosis
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