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To evaluate the efficacy and safety of lactulose combined with oral rehydration salts for intestinal preparation before colonoscopy

To evaluate the efficacy and safety of lactulose combined with oral rehydration salts for intestinal preparation before colonoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500098820
Enrollment
Unknown
Registered
2025-03-13
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

Bowel preparation for colonoscopy

Interventions

Sponsors

Beijing Friendship Hospital Pinggu Campus,Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.To undergo colonoscopy or treatment; 2.Patients with prior colonoscopy for oral pegylation intolerance and/or poor bowel And voluntarily chose lactulose as a laxative preparation; 3.Patients who volunteered to participate in the trial and signed informed consent;

Exclusion criteria

Exclusion criteria: 1.Patients with disturbance of consciousness; 2.Patients with present or suspected gastrointestinal perforation, intestinal obstruction and gastric retention; 3.Patients with active inflammatory bowel disease; 4.Patients with active gastrointestinal bleeding; 5.History of gastrointestinal surgery; 6.Patients with electrolyte disorders (including hyperkalemia, hypernatremia, hyponatremia); 7.Patients with serious heart disease, liver disease, kidney disease; 8.Other intestinal preparation drugs have been taken orally;

Design outcomes

Primary

MeasureTime frame
BBPS score;

Secondary

MeasureTime frame
There is no abdominal pain, abdominal distension, nausea and vomiting;

Countries

China

Contacts

Public ContactWang Rui

Beijing Pinggu District Hospitalcal University

wangrui.xiaomei@163.com+86 10 8999 9009

Outcome results

None listed

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