Clinical Trials Directory

Trials / Completed

CompletedNCT03849196

Effectiveness of Bisacodyl Suppository Agent for Dose Reduction of Low Dose PEG

Simultaneous Combination of Bisacodyl Suppository Agent and 1L Polyethylene Glycol Plus Ascorbic Acid is Not Inferior and Comfortable Regimen Compared With 2L Polyethylene Glycol Plus Ascorbic Acid: A Randomized Controlled Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
168 (actual)
Sponsor
Samsung Medical Center · Academic / Other
Sex
All
Age
20 Years – 70 Years
Healthy volunteers
Accepted

Summary

Proper bowel cleansing before colonoscopy is an important factor to increase the detection rate of lesions. Low volume polyethylene glycol (PEG) plus ascorbic (PEG-Asc) has reduced the dosage of previous bowel preparation agent, but it still presents discomfort to patients. The aim of this study was to confirm the efficacy and convenience of volume reduction of PEG-Asc by adding bisacodyl suppository at the same day by compared with conventional 2L PEG-Asc.

Detailed description

Eligibility criteria: outpatients between the ages of 20 and 70 years, who were scheduled for colonoscopy between August 2017 and January 2018 Exclusion criteria: patients with a history of gastrointestinal tract surgery, inflammatory bowel disease, severe active colitis, underlying chronic kidney disease, or pregnancy. Outcome measures: the Boston Bowel Preparation Scale (BBPS)

Conditions

Interventions

TypeNameDescription
DRUG2L PEG-AscPEG-Asc powder
DRUGBisacodyl 10Mg Suppositorybisacodyl 10 mg suppository
DRUG1L PEG-AscPEG-Asc powder

Timeline

Start date
2017-07-31
Primary completion
2018-01-30
Completion
2018-01-30
First posted
2019-02-21
Last updated
2019-02-21

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03849196. Inclusion in this directory is not an endorsement.