Trials / Completed
CompletedNCT05521685
Impact of EUS Guided Treatment of Gastric Varices
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 119 (actual)
- Sponsor
- Indiana University · Academic / Other
- Sex
- All
- Age
- 18 Years – 99 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the study is to determine the clinical impact of cyanoacrylate tissue adhesive treatment for Gastric Varices performed by Indiana University EUS physicians.
Detailed description
Using an IRB approved database (IU IRB#1209009522; NCT02037659), data collected from the database will be evaluated to identify complications, risk of rebleeding, death within 1 year of treatment, varices eradication and need for re-intervention associated with cyanoacrylate tissue adhesive (Dermabond) treatment performed by Indiana University Endoscopic Ultrasound (EUS) physicians.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Endoscopic Ultrasound (EUS) administration of cyanoacrylate tissue adhesive to control bleeding gastric varices | Subjects will have undergone treatment and been enrolled into the existing registry. |
Timeline
- Start date
- 2022-04-19
- Primary completion
- 2023-05-22
- Completion
- 2023-05-22
- First posted
- 2022-08-30
- Last updated
- 2024-01-12
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT05521685. Inclusion in this directory is not an endorsement.