A prospective observational study on cryobiopsy employing an ultrathin cryoprobe, a therapeutic bronchoscope, and a rigid bronchoscope to assess endobronchial lesions
Phase 3
Recruiting
- Conditions
- Endotracheal or endobronchial lesions
- Registration Number
- JPRN-UMIN000050607
- Lead Sponsor
- ational Hospital Organization Nagoya Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
1. Any serious, concomitant medical condition 2. Prior enrolment in this trial 3. Patients in whom a therapeutic bronchoscope and a 1.1-mm ultrathin cryoprobe were not used 4. Pregnancy 5. An inability to temporarily interrupt anticoagulant/antiplatelet agents 6. A bleeding tendency
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method