A Study Evaluating the Diagnostic Yield and Safety of the ProCore vs Conventional EBUS-TBNA Needle in Subjects With Suspected Sarcoidosis
Primary Purpose
Sarcoidosis
Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Procore biopsy needle
Conventional biopsy needle
Sponsored by
About this trial
This is an interventional diagnostic trial for Sarcoidosis
Eligibility Criteria
Inclusion Criteria: Patients meeting all the following criteria will be eligible for inclusion in the study:
- Age group of 18 to 75 years
- Clinicoradiological suspicion of sarcoidosis where EBUS-TBNA is being planned
- Enlarged hilar and 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:
- 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
- Bronchoscopy suite, PGIMER
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Procore needle
Conventional needle
Arm Description
EchoTip ProCore needle (Cook Medical Inc., Bloomington, Ind., USA)
Conventional 22-gauge EBUS-TBNA needle (Vizishot, Olympus, Japan)
Outcomes
Primary Outcome Measures
Proportion of patients with sarcoidosis diagnosed by EBUS-TBNA (Diagnostic yield)
The diagnostic yield is defined as the proportion of patients with a final diagnosis of sarcoidosis diagnosed by EBUS-TBNA
Secondary Outcome Measures
Number of patients with adequate EBUS-TBNA aspirate on cytology
Defined as preponderance of lymphocytes or a definite diagnosis (sarcoidosis, tuberculosis or others) on EBUS-TBNA aspirate
Incidence of adverse events related to EBUS-TBNA procedure in the two groups
Endobronchial bleeding, pneumothorax, hypoxemia, mediastinitis
Full Information
NCT ID
NCT03656003
First Posted
August 22, 2018
Last Updated
February 22, 2021
Sponsor
Postgraduate Institute of Medical Education and Research
1. Study Identification
Unique Protocol Identification Number
NCT03656003
Brief Title
A Study Evaluating the Diagnostic Yield and Safety of the ProCore vs Conventional EBUS-TBNA Needle in Subjects With Suspected Sarcoidosis
Official Title
A Study Evaluating the Diagnostic Yield and Safety of the ProCore vs Conventional EBUS-TBNA Needle in Subjects With Suspected Sarcoidosis
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
August 1, 2018 (Actual)
Primary Completion Date
July 31, 2019 (Actual)
Study Completion Date
July 31, 2019 (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
Yes
5. Study Description
Brief Summary
This study evaluates the yield and safety of two different needles for performing endobronchial ultrasound guided transbronchial needle aspiration (EBUS-TBNA) in patients with sarcoidosis. The two needles that will be compared will be the 22-gauge ProCore needle and the conventional 22-gauge EBUS-TBNA needle.
Detailed Description
Sarcoidosis is a multisystem disorder of unknown cause characterized by granulomatous inflammation involving various organ systems. The diagnosis is made on the basis of a suggestive clinicoradiological picture, histopathologic evidence of non-caseating granuloma, and exclusion of other known causes for granulomatous inflammation. As the lung and mediastinal lymph nodes are the most commonly involved structures in sarcoidosis, various bronchoscopic techniques like endobronchial biopsy (EBB), transbronchial biopsy (TBLB) and transbronchial needle aspiration (TBNA) are needed for tissue sampling.
Among the bronchoscopic techniques, TBNA of lymph nodes is a useful modality especially when combined with endobronchial and transbronchial biopsies. The efficacy and safety of conventional TBNA are well established. With the advent of endobronchial ultrasound (EBUS) in the last decade, this new technology has been widely used to guide transbronchial needle aspiration. The technique is minimally invasive and offers the additional advantage of choosing the appropriate node for sampling based on the vascularity, echogenicity and size. Studies subsequently have demonstrated the superiority of EBUS-TBNA over conventional TBNA.
As EBUS-TBNA is the standard procedure now for accessing intrathoracic lymph nodes, the technical aspects of the procedure need further investigation. Several aspects 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, and the distance travelled by the needle within the lymph node.
The EchoTip ProCore High Definition ultrasound biopsy needle (Cook Medical Inc., Bloomington, Ind., USA) is a novel needle that has been used mainly in sampling intra-abdominal lesions. It has a special bevel which allows a core biopsy along with aspiration of the lymph node material. In case of mediastinal lymph node enlargement due to malignancy, needle aspiration alone may yield sufficient material to identify malignant cells. However, in sarcoidosis, the core biopsy specimen obtained with the ProCore needle may potentially increase the identification of granulomas. The investigators hypothesize that the 22-gauge ProCore needle will have a higher yield in diagnosing intrathoracic lymphadenopathy due to sarcoidosis as compared to the conventional 22-gauge EBUS-TBNA needle. In this study, the investigators plan to evaluate the yield and safety of the 22-gauge ProCore needle as compared to 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
Outcomes Assessor
Allocation
Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Procore needle
Arm Type
Experimental
Arm Description
EchoTip ProCore needle (Cook Medical Inc., Bloomington, Ind., USA)
Arm Title
Conventional needle
Arm Type
Active Comparator
Arm Description
Conventional 22-gauge EBUS-TBNA needle (Vizishot, Olympus, Japan)
Intervention Type
Device
Intervention Name(s)
Procore biopsy needle
Intervention Description
EBUS-TBNA with the EchoTip ProCore needle (Cook Medical Inc., Bloomington, Ind., USA)
Intervention Type
Device
Intervention Name(s)
Conventional biopsy needle
Intervention Description
EBUS-TBNA with the conventional 22-gauge EBUS-TBNA needle (Vizishot, Olympus, Japan)
Primary Outcome Measure Information:
Title
Proportion of patients with sarcoidosis diagnosed by EBUS-TBNA (Diagnostic yield)
Description
The diagnostic yield is defined as the proportion of patients with a final diagnosis of sarcoidosis diagnosed by EBUS-TBNA
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Number of patients with adequate EBUS-TBNA aspirate on cytology
Description
Defined as preponderance of lymphocytes or a definite diagnosis (sarcoidosis, tuberculosis or others) on EBUS-TBNA aspirate
Time Frame
2 weeks
Title
Incidence of adverse events related to EBUS-TBNA procedure in the two groups
Description
Endobronchial bleeding, pneumothorax, hypoxemia, mediastinitis
Time Frame
1 week
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients meeting all the following criteria will be eligible for inclusion in the study:
Age group of 18 to 75 years
Clinicoradiological suspicion of sarcoidosis where EBUS-TBNA is being planned
Enlarged hilar and 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:
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ashutosh N Aggarwal
Organizational Affiliation
Professor & Head
Official's Role
Study Chair
Facility Information:
Facility Name
Bronchoscopy suite, PGIMER
City
Chandigarh
ZIP/Postal Code
160012
Country
India
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
33435733
Citation
Dhooria S, Sehgal IS, Prasad KT, Muthu V, Gupta N, Bal A, Ram B, Aggarwal AN, Agarwal R. Diagnostic yield and safety of the ProCore versus the standard EBUS-TBNA needle in subjects with suspected sarcoidosis. Expert Rev Med Devices. 2021 Feb;18(2):211-216. doi: 10.1080/17434440.2021.1876560. Epub 2021 Jan 22.
Results Reference
derived
Learn more about this trial
A Study Evaluating the Diagnostic Yield and Safety of the ProCore vs Conventional EBUS-TBNA Needle in Subjects With Suspected Sarcoidosis
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