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Efficacy and tolerability of low-volume polyethylene glycol solution (Moviprep) versus standard polyethylene glycol solution (Niflec) in bowel preparation for colonoscopy

Efficacy and tolerability of low-volume polyethylene glycol solution (Moviprep) versus standard polyethylene glycol solution (Niflec) in bowel preparation for colonoscopy - Efficacy and tolerability of low-volume polyethylene glycol solution (Moviprep) versus standard polyethylene glycol solution (Niflec) in bowel preparation for colonoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011505
Enrollment
100
Registered
2013-08-19
Start date
2013-08-21
Completion date
Unknown
Last updated
2026-06-29

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

Bowel preparation for colonoscopy using Niflec Bowel preparation for colonoscopy using Moviprep

Sponsors

Department of Endoscopy, Aichi Cancer Center Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Inpatients who are intend to resect colon polyp 2) Patients who agreed to participate in this research with written informed consent.

Exclusion criteria

Exclusion criteria: Patients with the following clinical features were excluded: significant cardiac, renal, hepatic, or metabolic co-morbidities, ascites, severe constipation (<2 bowel movement a week), known allergy to PEG-electrolyte solution, history of gastric stapling or bypass procedure, or a history of prior colonic or rectal surgery. Patients were excluded if there was a suspected diagnosis of intestinal obstruction because of advanced colorectal cancer.

Design outcomes

Primary

MeasureTime frame
Patient's Acceptance and Tolerability

Secondary

MeasureTime frame
Efficacy and Safety

Countries

Japan

Contacts

Public ContactMasahiro Tajika

Aichi Cancer Center Hospital Department of Endoscopy

mtajika@aichi-cc.jp052-762-6111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026