CompletedNot applicableNCT03656003
A Study Evaluating the Diagnostic Yield and Safety of the ProCore vs Conventional EBUS-TBNA Needle in Subjects With Suspected Sarcoidosis
Studying Sarcoidosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Post Graduate Institute of Medical Education and Research, Chandigarh
- Principal Investigator
- Ashutosh N AggarwalProfessor & Head
- Intervention
- Procore biopsy needle(device)
- Enrollment
- 100 target
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2018 – 2019
Study locations (1)
- Bronchoscopy suite, PGIMER, Chandigarh, India
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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