Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04902248

OTSC vs. Angiographic Embolization in Patients With Refractory Non-variceal Upper Gastrointestinal Bleeding

Led by Chinese University of Hong Kong · Updated on 2026-03-18

236

Participants Needed

5

Research Sites

261 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In the management of patients with acute upper non-variceal upper gastrointestinal bleeding, further bleeding is the most important adverse factor predictive of mortality. In the United Kingdom Audit on acute upper gastrointestinal bleeding, clinical evidence of further bleeding was reported in 13% of patients following the first endoscopy and 27% of them died. The use of OTSC has emerged as an alternative before angiographic embolization(TAE) which is often considered most definitive. We propose to define the algorithm in the management of patients with refractory bleeding from their peptic ulcers or other non variceal causes. We hypothesize that endoscopic use of OTSC compares favourably with TAE and both lead to similar outcomes. An equivalence of the two modalities may mean that endoscopic application of OTSC should be attempted before TAE as often we need to document further bleeds with endoscopy and a second treatment should be instituted at the same time.

CONDITIONS

Official Title

OTSC vs. Angiographic Embolization in Patients With Refractory Non-variceal Upper Gastrointestinal Bleeding

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with clear signs of acute upper gastrointestinal bleeding such as hematemesis, melena, or low blood pressure
  • Bleeding lesion confirmed by endoscopy (including ulcers, dieulafoy's lesion, or others)
  • Further bleeding (persistent or recurrent) after initial endoscopic treatment (thermal or hemoclips) as defined by an International Consensus Group
Not Eligible

You will not qualify if you...

  • Lack of full informed consent from the patient or a legal representative
  • Age under 18 years
  • Pregnant women
  • Lactating women
  • Known allergy to intravenous contrast agents

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 5 locations

1

Beijing friendship Hospital

Beijing, Beijing Municipality, China

Actively Recruiting

2

the First Affiliated Hospital of Nanchang University

Nanchang, Jiangxi, China

Actively Recruiting

3

Huaxi Hospital of Sichuan University

Chengdu, Sichuan, China

Actively Recruiting

4

Endoscopy Centre, Prince of Wales Hospital

Hong Kong, N.T., Hong Kong

Actively Recruiting

5

King Chulalongkorn Memorial Hospital

Bangkok, Bangkok, Thailand

Actively Recruiting

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Research Team

Y

Yau Wong James Lau, MD

CONTACT

Y

Yuanyuan yu, phd

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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