Clinical Trials Directory

Trials / Completed

CompletedNCT02037659

Dermabond Treatment for Gastric Variceal Bleeding

Endoscopic Ultrasound (EUS) Gastric Variceal Bleeding Database Repository

Status
Completed
Phase
Study type
Observational
Enrollment
98 (actual)
Sponsor
Indiana University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of having a database is to collect data related to endoscopic ultrasound procedures performed by Indiana University EUS physicians; specifically, for the treatment of gastric variceal bleeding This data will be used for research purposes only to determine the clinical impact of endoscopic ultrasound treatment of gastric variceal bleeding. The physicians will also be able to better understand the patient's condition and disease process that may lead to improved standard of care and improved patient management.

Detailed description

Clinical outcomes research is one of the strengths of the EUS group. As a group, the physicians need a tracking system for specific treatment modalities, and data to determine the impact of endoscopic ultrasound for patients with gastric variceal bleeding. Gastric variceal bleeding is a severe complication of portal hypertension with significant morbidity and mortality with limited therapeutic options. Currently, there is no database in existence for endoscopic ultrasound clinical research for specific procedures. Also, there is limited data regarding the outcome of endoscopic sclerotherapy with cyanoacrylate in the United States.

Conditions

Interventions

TypeNameDescription
PROCEDUREDermaBond treatment of Gastric VaricesEndoscopic Ultrasound (EUS) administration of DermaBond glue to control bleeding gastric varices.

Timeline

Start date
2012-12-01
Primary completion
2022-03-01
Completion
2022-03-01
First posted
2014-01-16
Last updated
2022-03-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02037659. Inclusion in this directory is not an endorsement.