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The effects of endoscopic conventional treatment and conventional treatment combined with Histoacryl glue on the rate of rebleeding in patients with acute nonvariceal upper gastrointestinal bleeding combined with coronary artery disease:A prospective randomized controlled study

The effects of endoscopic conventional treatment and conventional treatment combined with Histoacryl glue on the rate of rebleeding in patients with acute nonvariceal upper gastrointestinal bleeding combined with coronary artery disease:A prospective randomized controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080913
Enrollment
Unknown
Registered
2024-02-18
Start date
2024-02-20
Completion date
Unknown
Last updated
2024-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

acute nonvariceal upper gastrointestinal bleeding combined with coronary artery disease

Interventions

Conventional treatment group:combination therapy using epinephrine injection plus hemoclip and thrombin spray
experimental group:conventional treatment combined with spraying of Histoacryl glue

Sponsors

Beijing Anzhen Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: ? Patients = 18 years old; ?Patients was diagnosed with CAD (including acute coronary syndrome, post-stenting, post-coronary artery bypass grafting, stable ischemic heart disease treated with medication only) and received anti-platelet therapy before bleeding; ?Patients with clinical evidence of bleeding (such as hematemesis, melena, hematochezia, nasogastric tube aspirate with gross blood or coffee ground material); ?Active bleeding endoscopic stigmata (spurting or oozing bleeding or with a non- bleeding visible vessel ); ?Agree to accept the study protocol; ?Voluntarily sign informed consent.

Exclusion criteria

Exclusion criteria: ? Variceal upper gastrointestinal bleeding; ? Severe coagulation disorders caused by other causes; ? Contraindications for endoscopy (such as poor general condition, severe respiratory diseases, severe circulatory diseases, neck or spine abnormalities, etc); ? Participate in other clinical trials.

Design outcomes

Primary

MeasureTime frame
A composite of persistent bleeding, rebleeding within 7 days, or received other hemostatic treatment (e.g., transcatheter arterial embolization, surgery);

Secondary

MeasureTime frame
Units of transfusion ;Death;

Countries

China

Contacts

Public ContactJie Zhang

Beijing Anzhen Hospital,Capital Medical University

zhangjie4155@126.com+86 189 1166 2871

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026