A Safety and Efficacy Evaluation of 3 Bowel Preparations in the Pediatric Population

ClinicalTrials.gov ID: NCT00425594

Public ClinicalTrials.gov record NCT00425594. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

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ClinicalTrials.gov public records Last synced Oct 22, 2026, 1:32 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This randomized, parallel, multi-center, single-blind study is designed to compare the safety and efficacy of 3 bowel preparations in pediatric subjects scheduled to undergo a colonoscopy for a routinely accepted indication.

Study identification

NCT ID: NCT00425594
Recruitment status: Completed
Study type: Interventional
Phase: Phase 4
Lead sponsor: Braintree Laboratories; Industry
Enrollment: 150 participants

Conditions and interventions

Conditions

Colonoscopy

Interventions

Drug

Eligibility (public fields only)

Age range: 6 Years to 16 Years
Sex: All
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Jan 2007 (Type not available)
Primary completion: May 2007 (Actual)
Completion: May 2007 (Actual)
Last update posted: Dec 27, 2007

2007

United States locations

U.S. sites: 26
U.S. states: 21
U.S. cities: 26

Facility	City	State	ZIP	Site status
Not listed	Birmingham	Alabama	35233	—
Not listed	Mobile	Alabama	36604	—
Not listed	Tuscaloosa	Alabama	35406	—
Not listed	Phoenix	Arizona	85016	—
Not listed	Little Rock	Arkansas	72202	—
Not listed	San Francisco	California	94143	—
Not listed	Gainesville	Florida	32610	—
Not listed	Orlando	Florida	32801	—
Not listed	Park Ridge	Illinois	60068	—
Not listed	Indianapolis	Indiana	46202	—
Not listed	Boston	Massachusetts	02114	—
Not listed	Minneapolis	Minnesota	55455	—
Not listed	Jackson	Mississippi	39216	—
Not listed	Omaha	Nebraska	68198	—
Not listed	Las Vegas	Nevada	89109	—
Not listed	Morristown	New Jersey	07962	—
Not listed	Buffalo	New York	14222	—
Not listed	Cleveland	Ohio	44106	—
Not listed	Columbus	Ohio	43205	—
Not listed	Lancaster	Pennsylvania	17604	—
Not listed	Columbia	South Carolina	29203	—
Not listed	Houston	Texas	77030	—
Not listed	Temple	Texas	76508	—
Not listed	Salt Lake City	Utah	84113	—
Not listed	Burlington	Vermont	05401	—
Not listed	Milwaukee	Wisconsin	53226	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT00425594, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Dec 27, 2007 · Synced Oct 22, 2026

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00425594 live on ClinicalTrials.gov.

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