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NCT04468737 Clinical Trial

Effect of Inadequate Bowel Preparation on Urgent Colonoscopy in Patients With PPB.

Bowel Preparation Clinical Trial

— PPB  

Official title:
Effect of Inadequate Bowel Preparation on Urgent Colonoscopy in Patients With Post-polypectomy Bleeding (PPB): A Descriptive Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04468737
Other study ID # PPB-1.0
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2010
Est. completion date June 15, 2020

Study information
Verified date June 2020
Source Ningbo No. 1 Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study was to explore the effect of abbreviated bowel preparation on repeated colonoscopy in patients with PPB.

Recruitment information / eligibility
Status Completed
Enrollment 34
Est. completion date June 15, 2020
Est. primary completion date June 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

patients with bleeding after polypectomy patients treated with colonoscopy within 24 hours after bleeding patients who did not receive adequate bowel preparation (oral laxatives).

Exclusion Criteria:

patients whose main outcome indicators were not clearly described patients whose baseline characteristics were missing.

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Bowel preparation
Observe patients who undergo bowel preparation by enema or irrigation

Locations
Country Name City State
China Ningbo first hospital Ningbo Zhejiang

Sponsors (1)
Lead Sponsor Collaborator
Ningbo No. 1 Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Diagnostic rate the rate of identified the origin of the bleeding 1 Day of colonoscopy
Secondary Ileocaecal intubation rate the rate of colonoscopy entering the cecum 1 Day of colonoscopy
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