NCT03656003View on ClinicalTrials.gov

A Study Evaluating the Diagnostic Yield and Safety of the ProCore vs Conventional EBUS-TBNA Needle in Subjects With Suspected Sarcoidosis

NACompletedINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

August 1, 2018

Primary Completion Date

July 31, 2019

Study Completion Date

July 31, 2019

Conditions
Sarcoidosis
Interventions
DEVICE

Procore biopsy needle

EBUS-TBNA with the EchoTip ProCore needle (Cook Medical Inc., Bloomington, Ind., USA)

DEVICE

Conventional biopsy needle

EBUS-TBNA with the conventional 22-gauge EBUS-TBNA needle (Vizishot, Olympus, Japan)

Trial Locations (1)

160012

Bronchoscopy suite, PGIMER, Chandigarh

All Listed Sponsors
lead

Post Graduate Institute of Medical Education and Research, Chandigarh

OTHER

NCT03656003 - A Study Evaluating the Diagnostic Yield and Safety of the ProCore vs Conventional EBUS-TBNA Needle in Subjects With Suspected Sarcoidosis | Biotech Hunter | Biotech Hunter