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Clinical Research on Individualized Bowel Preparation with Lactulose

Clinical Research on Individualized Bowel Preparation with Lactulose

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106045
Enrollment
Unknown
Registered
2025-07-16
Start date
2025-06-02
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

None

Interventions

Lactulose group:Pour 200 ml of lactulose oral solution into a 1 L measuring cup and dilute with warm water to 0.5 L to prepare the lactulose mixture. Take the mixture in several doses within 30 minute
PEG group:Take the 3L polyethylene glycol solution in divided doses.

Sponsors

The Central Hospital of Wuhan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years, regardless of gender; 2. Signed written informed consent; 3. Patients who have indications for colonoscopy and are undergoing diagnostic colonoscopy; 4. Willing to accept lactulose as the bowel preparation agent.

Exclusion criteria

Exclusion criteria: 1. Aged <18 years; 2. Refusal or failure to sign the informed consent; 3. Pregnant, planning to become pregnant, or breastfeeding women; 4. Allergy or intolerance to PEG or lactulose; 5. Presence of any contraindications to colonoscopy; 6. Patients with a history of colectomy or ileostomy.

Design outcomes

Primary

MeasureTime frame
The Boston Bowel Preparation Scale Score;

Countries

Chian

Contacts

Public ContactHu Zhang

The Central Hospital of Wuhan

425084095@qq.com+86 135 4528 1634

Outcome results

None listed

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