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Early oral feeding in patients with acute non-variceal upper gastrointestinal bleeding: a prospective, randomized controlled trial

Construction and application of integrated rapid doctor-nurse rapid rehabilitation system for patients with acute non-variceal upper gastrointestinal bleeding treated by endoscope

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061985
Enrollment
Unknown
Registered
2022-07-15
Start date
2022-07-01
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Acute non-variceal upper gastrointestinal bleeding

Interventions

Control group:conventional oral feeding

Sponsors

The First Affiliated Hospital of Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. The age of the patient is >= 18 years old; 2. Diagnosed by endoscopy, in line with the diagnostic criteria for non-variceal upper gastrointestinal bleeding; 3. The score RS of patients who did not receive endoscopic hemostatic treatment during hospitalization was <= 3 points; the score R-RS of patients who received endoscopic hemostatic treatment was less than 5 points; 4. Possess basic Chinese reading and writing skills, normal understanding and expression skills, and barrier-free communication; 5. Patient's informed consent.

Exclusion criteria

Exclusion criteria: 1. Gastrointestinal malignant tumors; 2. Patients admitted to the hospital due to other diseases, and patients with upper gastrointestinal bleeding in the hospital; 3. People with coagulation dysfunction; 4. Patients with diabetes mellitus, or with heart, lung, brain, liver, kidney and other severe organ dysfunction who cannot cooperate with intervention; 5. Patients with mental abnormalities who cannot cooperate with the intervention.

Design outcomes

Primary

MeasureTime frame
first exhaust time;first dejection time;hospital stay;Infusion quantity;hemoglobin;albumin;sodium;potassium;Re-clinical intervention;

Secondary

MeasureTime frame
rebleeding rate;death rate;hospitalization expense;anxiety and depression score;quality of life;patient’s satisfaction;

Countries

China

Contacts

Public ContactZehao Zhuang

The First Affiliated Hospital of Fujian Medical University

zhuang203@gmail.com+86 13178032412

Outcome results

None listed

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