Application of Linaclotide Capsule in Bowel Preparation for Colonoscopy

NCT05291325 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1607

Last updated 2024-06-20

No results posted yet for this study

Summary

The clinical purpose of this study was to investigate whether the adjuvant application of linaclotide in bowel preparation for colonoscopy could improve the quality of bowel preparation or reduce the dosage of laxatives.

Conditions

  • Bowel Preparation for Colonoscopy

Interventions

DRUG

3L PEG + Linaclotide

Before colonoscopy, particpant take linaclotide capsules for 3 days (1 tablet should be taken at least 30 minutes before the first meal every day). Particpant take 1500ml polyethylene glycol electrolyte solution within 1.5 hours from 20 p.m the night before the examination; and repeat the same dose of polyethylene glycol electrolyte solution 4-6 hours before colonoscopy.

DRUG

3L PEG

Particpant take 1500ml polyethylene glycol electrolyte solution within 1.5 hours from 20 p.m the night before the examination; and repeat the same dose of polyethylene glycol electrolyte solution 4-6 hours before colonoscopy.

DRUG

2L PEG + Linaclotide

Before colonoscopy, particpant take linaclotide capsules for 3 days (1 tablet should be taken at least 30 minutes before the first meal every day). Particpant take 1000ml polyethylene glycol electrolyte solution within 1 hours from 20 p.m the night before the examination; and repeat the same dose of polyethylene glycol electrolyte solution 4-6 hours before colonoscopy.

Sponsors & Collaborators

  • Shanxi Provincial People's Hospital

    collaborator OTHER_GOV
  • 900 Hospital of Joint Logistics Support Force of PLA

    collaborator OTHER
  • Ruijin Hospital

    collaborator OTHER
  • The First Affiliated Hospital of Nanchang University

    collaborator OTHER
  • Qilu Hospital of Shandong University

    collaborator OTHER
  • The Affiliated Hospital of Qingdao University

    collaborator OTHER
  • The Third Affiliated Hospital of Wenzhou Medical University

    collaborator OTHER
  • Affiliated Yueqing Hospital of Wenzhou Medical University

    collaborator OTHER
  • The First Affiliated Hospital of Soochow University

    collaborator OTHER
  • The 7th Medical Center of the PLA General Hospital

    collaborator UNKNOWN
  • The First Hospital of Jilin University

    collaborator OTHER
  • The Second Hospital of Hebei Medical University

    collaborator OTHER
  • The Affiliated Hospital of Inner Mongolia Medical University

    collaborator OTHER
  • The Second Affiliated Hospital of Dalian Medical University

    collaborator OTHER
  • Ningxia Medical University General Hospital

    collaborator UNKNOWN
  • Affiliated Hospital of Qinghai University

    collaborator OTHER
  • Yunnan First People's Hospital

    collaborator UNKNOWN
  • Xiangya Second Hospital, Central South University

    collaborator UNKNOWN
  • Shanghai Zhongshan Hospital

    collaborator OTHER
  • Daping Hospital, Army Military Medical University

    collaborator UNKNOWN
  • Zunyi Medical College

    collaborator OTHER
  • Huizhou Municipal Central Hospital

    collaborator OTHER
  • Affiliated Hospital of Southwest Medical University

    collaborator OTHER
  • The First Hospital of Shihezi University

    collaborator UNKNOWN
  • Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

    collaborator OTHER
  • Tangdu Hospital of Air Force Military Medical University

    collaborator UNKNOWN
  • Changhai Hospital

    lead OTHER

Principal Investigators

  • Zhaoshen Li · Changhai Hospital

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-05-25
Primary Completion
2023-08-30
Completion
2024-04-28

Countries

  • China

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05291325 on ClinicalTrials.gov