OTSC vs. Angiographic Embolization in Patients With Refractory Non-variceal Upper Gastrointestinal Bleeding
Launched by CHINESE UNIVERSITY OF HONG KONG · May 25, 2021
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying two different methods for treating patients who have serious bleeding in the upper part of the digestive system, specifically when traditional treatments are not effective. The two methods being compared are OTSC, which is a technique that involves placing a special clip to stop the bleeding, and angiographic embolization (TAE), a procedure that blocks the blood vessels causing the bleeding. The goal is to find out if using OTSC first can provide similar results to TAE, potentially allowing for a quicker and less invasive treatment.
To participate in this trial, patients should be adults aged 65 and older who show clear signs of bleeding, such as vomiting blood or having dark, tarry stools. They should have a documented bleeding problem identified during an endoscopy, which is a procedure that allows doctors to see inside the stomach and digestive tract. Participants can expect to undergo either of the two treatments and be monitored for their recovery. It's important to note that this study is currently recruiting, and interested patients will need to provide their consent or have a family member do so if they are unable.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Patients presented with overt signs of acute upper gastrointestinal bleeding (hematemesis, melena and/or hypotension) 2. documented bleeding lesion at endoscopy (ulcer, dieulafoy's lesion and others), further bleeds (persistent or recurrent) after endoscopic hemostasis (thermal or hemoclips) as defined by an International Consensus Group
- Exclusion Criteria:
- • 1. without a full informed consent from the patient or his next of kin
- • 2. Age \<18 years
- • 3. Pregnant
- • 4. Lactating women
- • 5. patients with known allergy to intravenous contrast
About Chinese University Of Hong Kong
The Chinese University of Hong Kong (CUHK) is a prestigious research institution renowned for its commitment to advancing medical science and improving healthcare outcomes. As a clinical trial sponsor, CUHK leverages its extensive academic resources and interdisciplinary expertise to conduct innovative research that addresses critical health challenges. The university fosters collaboration among leading researchers, healthcare professionals, and industry partners, ensuring rigorous study design and implementation. CUHK is dedicated to upholding the highest ethical standards in clinical research, with a focus on translating findings into tangible benefits for patients and the broader community.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Bangkok, , Thailand
Chengdu, Sichuan, China
Beijing, Beijing, China
Nanchang, Jiangxi, China
Hong Kong, N.T., Hong Kong
Patients applied
Trial Officials
Yau Wong James Lau, MD
Principal Investigator
The Chinese University of HongKong
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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