NCT05187312
Recruiting
Not Applicable
Research Registry for Endoscopic Treatment and Diagnostics
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Cholangiocarcinoma
- Sponsor
- Region Stockholm
- Enrollment
- 1000
- Locations
- 1
- Primary Endpoint
- Diagnostic yield
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
Observational registry including endoscopic diagnostic and therapeutic interventions in the gastrointestinal tract
Investigators
Eligibility Criteria
Inclusion Criteria
- •Clinical indication for endoscopic intervention/procedure
Exclusion Criteria
- •No informed consent
- •Age \<18 years
Outcomes
Primary Outcomes
Diagnostic yield
Time Frame: 1-year follow up
Diagnostic yield after tissue sampling
Adverse events
Time Frame: 30-days and 60-days post-procedure
Incidence of Adverse events following endoscopic procedures. Measured as percentage of individuals with an adverse event
Study Sites (1)
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