Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02124447

Single Center Comparison of 4 FDA Approved, Commercially Available Bowel Purgatives for Colonoscopy

Comparison of Efficacy and Patient Tolerability of Four Commercially Available Bowel Purgatives for Screening and Surveillance Colonoscopy: A Single Tertiary Medical Center Experience.

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Medical College of Wisconsin · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

This will be a 4-way comparison to prospectively evaluate the efficacy and patient tolerability of four commercially available bowel preparations among patients undergoing colonoscopy for screening and surveillance in a single tertiary academic medical center.

Detailed description

We will randomize 300 consecutive patients undergoing colonoscopy for screening or surveillance purposes to receive one of four bowel purgatives. These purgatives include 1. Split dose 4 liter polyethylene glycol with electrolytes (PEG+E): Brand name GoLytely 2. Split dose 2 liter polyethylene glycol with ascorbic acid (PEG+Asc): Brand name: MoviPrep 3. Split dose sodium picosulfate, magnesium oxide, and anhydrous citric acid (P+MC): Brand name Prepopik 4. Split dose sodium sulfate, magnesium sulfate, and potassium sulfate solution (sulfate): Brand name Suprep

Conditions

Interventions

TypeNameDescription
DRUGPEG+ESplit dose 4 liter polyethylene glycol with electrolytes
DRUGPEG+AscSplit dose 2 liter polyethylene glycol with ascorbic acid
DRUGP+MCSplit dose sodium picosulfate, magnesium oxide, and anhydrous citric acid
DRUGsulfateSplit dose sodium sulfate, magnesium sulfate, and potassium sulfate solution

Timeline

Start date
2014-06-01
Primary completion
2014-08-01
Completion
2015-06-01
First posted
2014-04-28
Last updated
2015-07-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02124447. Inclusion in this directory is not an endorsement.