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NCT01169220 Clinical Trial

Bowel Preparation for Inpatient Colonoscopy

Colon Cancer Clinical Trial

Official title:
Single Blind, Randomized, Controlled Trial of Conventional Versus Split-Dose Bowel Preparation for Inpatient Colonoscopy

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01169220
Other study ID # 10-041
Secondary ID
Status Completed
Phase Phase 4
First received July 20, 2010
Last updated October 3, 2017
Start date July 2010
Est. completion date January 2014

Study information
Verified date October 2017
Source Santa Clara Valley Health & Hospital System
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will compare two strategies for bowel cleansing prior to inpatient colonoscopy: the entire preparation taken the night before the procedure versus half the preparation taken the night before the procedure, and the other half taken the morning of the procedure.

Recruitment information / eligibility
Status Completed
Enrollment 55
Est. completion date January 2014
Est. primary completion date January 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- any diagnosis for which colonoscopy is indicated

Exclusion Criteria:

- ileus

- severe colitis/toxic megacolon

- gastric retention

- bowel perforation

- gastrointestinal obstruction

- gastroparesis that precludes oral bowel preparation

- pregnant or lactating women

- allergy to polyethylene glycol.

- unable to give consent

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Go-Lytely
Bowel cleansing agent
• Go Lytely
Bowel cleansing agent

Locations
Country Name City State
United States Santa Clara Valley Medical Center San Jose California

Sponsors (1)
Lead Sponsor Collaborator
Santa Clara Valley Health & Hospital System

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Quality of colon cleansing 24 hours from study enrollment
Secondary Patient satisfaction 24 hours from study enrollment
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