Skip to content

Study of intestinal preparation or not on colonoscopy results in patients with acute lower gastrointestinal hemorrhage

Study of intestinal preparation or not on colonoscopy results in patients with acute lower gastrointestinal hemorrhage

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050456
Enrollment
Unknown
Registered
2021-08-27
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Severe acute lower gastrointestinal bleeding (SALGIB)

Interventions

Control group:None
Experimental group:PEG bowel preparation before colonoscopy

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years; 2. Patients with new acute lower gastrointestinal hemorrhage, or those who come to the hospital within 24 hours after the correction of acute lower gastrointestinal hemorrhage and hemorrhagic shock. New onset of acute lower gastrointestinal bleeding: blood in the stool with any of the following manifestations within 24 hours: (1) Hematochezia within 8 hours, and Oakland score > 8; (2) Hemorrhagic shock: shock index > 1; (3) Heart rate > 100 beats/min and systolic blood pressure 30 mm Hg from the usual level in the absence of vasoactive drugs); (4) The hemoglobin decreased by more than 30 g/L within 24 hours (the hematocrit decreased by about 9%); 3. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Previous diagnosis of inflammatory bowel disease (ulcerative colitis or Crohn's disease); 2. Patients with suspected gastrointestinal perforation and peritonitis; 3. Those who have been diagnosed with intestinal malignant tumor in the past; 4. History of total colectomy; 5. Combined with primary coagulation disorders, such as hemophilia; 6. Pregnant and lactating patients.

Design outcomes

Primary

MeasureTime frame
Detection rate of recent bleeding lesions;

Countries

China

Contacts

Public ContactXiao Xue

West China Hospital, Sichuan University

xiaoxue@wchscu.cn+86 15982175701

Outcome results

None listed

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