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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04150133
Other study ID # foodprep2019
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 21, 2019
Est. completion date October 1, 2021

Study information

Verified date March 2022
Source Hillmont GI
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The Efficacy of Clenpiq utilized per FDA labeling, with a low residue diet the day before colonoscopy.


Description:

This study proposes to assess the use of a low residue diet of a prescribed nature the day before colonoscopy for breakfast, lunch and early dinner. Clinical outcomes utilizing the low residue diet will be compared to the Food and Drug Administration (FDA) approved split dose labeling, including the traditional clear liquid diet the day before colonoscopy utilizing the Clenpiq (Ferring Pharmaceuticals) bowel preparation.


Recruitment information / eligibility

Status Completed
Enrollment 154
Est. completion date October 1, 2021
Est. primary completion date January 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - All subjects age 18-80 requiring colonoscopy for appropriate indications Exclusion Criteria: - Active diarrhea (Greater than 3 unformed stools daily) - Constipation (Less than 3 spontaneous bowel movements per week) Each within 2 weeks of the scheduled Colonoscopy. Additional exclusion criteria would include; - Subjects with a history of inflammatory bowel disease - Colonic resection of any length - Pregnant women - American Society of Anesthesiologists (ASA) score greater than 3 - Body Mass Index (BMI) greater than 50 - Previous reaction to this bowel preparation or contraindications to taking Clenpiq per the package labeling guidelines. - Subjects unable to give their own informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Low Residue Diet
Variable cohort will eat 3 low residue meals on the day prior to their planned colonoscopy

Locations

Country Name City State
United States Hillmont GI Flourtown Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
Hillmont GI Ferring Pharmaceuticals

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Statistical equivalence of the clear liquid and low residue cohorts Using the Boston Bowel Preparation Score, the 3 sections of the colon will be graded on adequacy of preparation at the colonoscopy During Colonoscopy Up to 24 hours
Secondary Polyp Detection Rate Number of polyps detected and removed per total number of patients in each arm Post Procedure Up to 24 hours
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