An RCT of 19G EBUS-TBNA Needle in Suspected Sarcoidosis (GUESS)
Primary Purpose
Sarcoidosis
Status
Unknown status
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
19 gauge needle
22 gauge needle
Sponsored by
About this trial
This is an interventional diagnostic trial for Sarcoidosis
Eligibility Criteria
Inclusion Criteria: All the following
- Age at least 18 years
- Clinicoradiological suspicion of sarcoidosis where EBUS-TBNA is being planned
- Enlarged bilateral hilar and/or mediastinal lymph nodes >10 mm (any axis) on computed tomography of the chest
- Ability to provide informed consent to participate in the study.
Exclusion Criteria: Patients with any of the following will be excluded
- Asymmetric lymph nodes
- Lymph nodes with significant hypodense areas suggestive of necrosis
- Tuberculin skin test >10 mm
- Hypoxemia (SpO2 <92% on FiO2 of 0.3)
- Treatment with systemic glucocorticoids for >2 weeks in the preceding three months
- Diagnosis of sarcoidosis possible with another minimally invasive technique such as skin biopsy or peripheral lymph node biopsy
- Failure to provide informed consent.
Sites / Locations
- PGIMERRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
19G
22G
Arm Description
19 gauge EBUS-TBNA needle
22 gauge EBUS-TBNA needle
Outcomes
Primary Outcome Measures
Diagnostic yield of EBUS-TBNA samples
Specimen showing epithelioid cell granulomas or collection of epithelioid cells with a giant cell (or asteroid body or Schaumann body).
Secondary Outcome Measures
Adequacy of EBUS-TBNA samples
Specimen shows a preponderance of lymphocytes or is diagnostic
Complication rate
Complication associated with EBUS-TBNA procedure
Cough visual analog scale (VAS)
Operator-rated visual analog scale (VAS) score for the intensity of subject's cough
Operator VAS
VAS score for ease of performance of the needle puncture and aspiration rated by the operator
Full Information
NCT ID
NCT04770948
First Posted
February 22, 2021
Last Updated
February 22, 2021
Sponsor
Postgraduate Institute of Medical Education and Research
Collaborators
AIIMS, New Delhi, Apollo Hospitals, Bengaluru, Jaipur Golden Hospital, New Delhi, Rajiv Gandhi Cancer Institute, New Delhi, Institute of Pulmonology, Medical Research, and Development, Mumbai, AIIMS, Bhopal, Asian Institute of Gastroenterology, Hyderabad, Yashoda Hospitals, Hyderabad, City Clinic and Bhailal Amin General Hospital, Vadodara
1. Study Identification
Unique Protocol Identification Number
NCT04770948
Brief Title
An RCT of 19G EBUS-TBNA Needle in Suspected Sarcoidosis
Acronym
GUESS
Official Title
A Study Evaluating the Diagnostic Yield and Safety of the 19-GaUge vs 22-Gauge EBUS-TBNA Needle in Subjects With Suspected Sarcoidosis (GUESS)
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 2021 (Anticipated)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Postgraduate Institute of Medical Education and Research
Collaborators
AIIMS, New Delhi, Apollo Hospitals, Bengaluru, Jaipur Golden Hospital, New Delhi, Rajiv Gandhi Cancer Institute, New Delhi, Institute of Pulmonology, Medical Research, and Development, Mumbai, AIIMS, Bhopal, Asian Institute of Gastroenterology, Hyderabad, Yashoda Hospitals, Hyderabad, City Clinic and Bhailal Amin General Hospital, Vadodara
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
Sarcoidosis is an idiopathic disorder characterized by granulomatous inflammation involving various organ systems. The lung and mediastinal lymph nodes are the most commonly involved structures in sarcoidosis. In the presence of intrathoracic lymph nodes, transbronchial needle aspiration (TBNA) is a useful diagnostic modality, which is now guided using endobronchial ultrasound (EBUS).
We hypothesize that the 19-gauge EBUS-TBNA needle will have a higher yield as compared to the conventional 22-gauge EBUS-TBNA needle in intrathoracic lymphadenopathy due to sarcoidosis. In this study, we plan to evaluate the yield and safety of the 19-gauge needle vs. the conventional 22-gauge EBUS-TBNA needle in patients with sarcoidosis.
Detailed Description
Sarcoidosis is an idiopathic disorder characterized by granulomatous inflammation involving various organ systems. The disease is diagnosed based on a suggestive clinicoradiological picture and the presence of non-caseating granulomas in the involved organ, after excluding known causes of granulomatous inflammation. The lung and mediastinal lymph nodes are the most commonly involved structures in sarcoidosis. Various bronchoscopic techniques such as endobronchial biopsy (EBB), transbronchial biopsy (TBLB) and transbronchial needle aspiration (TBNA) are commonly used for acquiring tissue samples.
In the presence of intrathoracic lymph nodes, TBNA is a useful diagnostic modality, especially when combined with endobronchial and transbronchial biopsies. At most centers, TBNA is now guided using endobronchial ultrasound (EBUS). The technique is minimally invasive and also offers the advantage of a selection of the appropriate node for sampling based on the ultrasonographic characteristics. Several studies have demonstrated the superiority of EBUS-TBNA over conventional TBNA (TBNA performed without real-time guidance).
Several technical aspects of EBUS-TBNA have been studied to optimize the yield including the number of aspirations or passes required per lymph node station, needle gauge (21 vs. 22 gauge), suction pressure, the distance travelled by the needle within the lymph node, the number of needle agitations required during a pass, and others.
The novel 19-G Vizishot FLEX EBUS needle (Olympus) is composed of a more flexible material (nitinol) than the 22-G EBUS needle. This allows it to have a larger inner diameter with the same outer diameter as a 22-G EBUS needle. Recent studies have shown that the 19-G needle is safe and has a comparable yield to smaller bore needles. In case of suspected lymphadenopathy due to malignant disorders, aspiration using smaller gauge needles may yield sufficient material for diagnosis. However, in sarcoidosis, larger nodal tissue obtained with a thicker bore needle, the 19-gauge needle, may potentially increase the identification of granulomas. We hypothesize that the 19-gauge EBUS-TBNA needle will have a higher yield as compared to the conventional 22-gauge EBUS-TBNA needle in intrathoracic lymphadenopathy due to sarcoidosis. In this study, we plan to evaluate the yield and safety of the 19-gauge needle vs. the conventional 22-gauge EBUS-TBNA needle in patients with sarcoidosis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sarcoidosis
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
400 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
19G
Arm Type
Experimental
Arm Description
19 gauge EBUS-TBNA needle
Arm Title
22G
Arm Type
Active Comparator
Arm Description
22 gauge EBUS-TBNA needle
Intervention Type
Device
Intervention Name(s)
19 gauge needle
Intervention Description
EBUS-TBNA performed using 19G needle
Intervention Type
Device
Intervention Name(s)
22 gauge needle
Intervention Description
EBUS-TBNA performed using 22G needle
Primary Outcome Measure Information:
Title
Diagnostic yield of EBUS-TBNA samples
Description
Specimen showing epithelioid cell granulomas or collection of epithelioid cells with a giant cell (or asteroid body or Schaumann body).
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Adequacy of EBUS-TBNA samples
Description
Specimen shows a preponderance of lymphocytes or is diagnostic
Time Frame
7 days
Title
Complication rate
Description
Complication associated with EBUS-TBNA procedure
Time Frame
7 days
Title
Cough visual analog scale (VAS)
Description
Operator-rated visual analog scale (VAS) score for the intensity of subject's cough
Time Frame
1 day
Title
Operator VAS
Description
VAS score for ease of performance of the needle puncture and aspiration rated by the operator
Time Frame
1 day
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All the following
Age at least 18 years
Clinicoradiological suspicion of sarcoidosis where EBUS-TBNA is being planned
Enlarged bilateral hilar and/or mediastinal lymph nodes >10 mm (any axis) on computed tomography of the chest
Ability to provide informed consent to participate in the study.
Exclusion Criteria: Patients with any of the following will be excluded
Asymmetric lymph nodes
Lymph nodes with significant hypodense areas suggestive of necrosis
Tuberculin skin test >10 mm
Hypoxemia (SpO2 <92% on FiO2 of 0.3)
Treatment with systemic glucocorticoids for >2 weeks in the preceding three months
Diagnosis of sarcoidosis possible with another minimally invasive technique such as skin biopsy or peripheral lymph node biopsy
Failure to provide informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sahajal Dhooria, MD, DM
Phone
7087002015
Email
sahajal@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Ritesh Agarwal, MD, DM
Phone
7087007625
Email
riteshpgi@gmail.com
Facility Information:
Facility Name
PGIMER
City
Chandigarh
ZIP/Postal Code
160012
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sahajal Dhooria, MD, DM
Phone
7087002015
Email
sahajal@gmail.com
First Name & Middle Initial & Last Name & Degree
Ritesh Agarwal, MD, DM
Phone
7087007625
Email
riteshpgi@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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An RCT of 19G EBUS-TBNA Needle in Suspected Sarcoidosis
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