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

Construction and application of medical care integration of rapid rehabilitation system for patients with acute upper gastrointestinal bleeding treated by endoscopy

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200060316
Enrollment
Unknown
Registered
2022-05-28
Start date
2022-05-15
Completion date
Unknown
Last updated
2024-05-06

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

Group 1 :Medical and nursing integrated rapid recovery system
Group 2:Current hospital treatment and care practices

Sponsors

The First Hospital of Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Patients who were first diagnosed with acute upper gastrointestinal bleeding on admission; 2. Age >= 18 years old; 3. Admitted to hospital by emergency department or gastroenterology department; 4. The patient is conscious or unconscious, but accompanied by family members or relatives and friends; 5. The patient did not receive endoscopic treatment and the RS score was <= 4 or the patient received endoscopic hemostatic treatment during hospitalization and the modified RS score was < 5; 6. Possess basic Chinese reading and writing skills, normal understanding and expression skills, and barrier-free communication; 7. The patient or his legal representative signs the informed consent.

Exclusion criteria

Exclusion criteria: 1. Diagnosed as acute variceal upper gastrointestinal bleeding after endoscopy; 2. Patients who are pregnant or breastfeeding; 3. Gastrointestinal malignant tumors; 4. People with coagulation dysfunction; 5. Patients with mental abnormalities who cannot cooperate with the intervention; 6. Patients with heart, lung, brain, liver, kidney and other severe organ dysfunction who cannot cooperate with intervention.

Design outcomes

Primary

MeasureTime frame
Time of in-hospital transfer;Time of the patient's first meal after endoscopic treatment;Time of patient's hospitalization;Patient's hospitalization costs;Patients' satisfaction with nursing care;

Secondary

MeasureTime frame
Rate of rebleeding during hospitalization;Mortality rate during hospitalisation;Patient's recovery of gastrointestinal function: number and degree of abdominal distension and pain;

Countries

China

Contacts

Public ContactZhuang Zehao

School of Nursing, Fujian Medical University

zehaozhuang@fjmu.edu.cn+86 13178032412

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026