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NCT00164151

A Comparison of the Efficacy and Safety of Two Bowel Preparations: HalfLytely® (2L NuLYTELY and 20 mg Bisacodyl), and Visicol™ Prior To Colonoscopy.

Completed Phase 3 Last updated 6 February 2013
What this trial tests

Phase 3 trial testing HalfLytely in Colonoscopy in 60 participants. Completed.

Timeline
1 June 2001
Primary endpoint
1 May 2002

Quick facts

Lead sponsorBraintree Laboratories
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designfactorial
Maskingsingle
Enrollment60
Start date1 June 2001
Primary completion1 May 2002
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Braintree Laboratories — full company profile →

Who can join

18 and older, any sex, with Colonoscopy.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The objective of this study is to determine the efficacy and safety of HalfLytely as compared to Visicol as bowel preparations before colonoscopic examination.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Drug and Clinical Candidate Drug Data in ChEMBL.
    Hunter FMI, Ioannidis H, Bento AP, Bosc N, et al · · 2025 · cited 3× · PMID 40971497 · DOI 10.1021/acs.jmedchem.5c00920

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Other recruiting trials for Colonoscopy

Currently open trials in the same condition.

Other Braintree Laboratories trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00164151.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing