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COMPLETED Phase 3

BLI-800-301: BLI-800 vs an Active Control Bowel Preparation in Adult Subjects Undergoing Colonoscopy

NCT00503607 · View on ClinicalTrials.gov ↗

Study Summary

This is a randomized, parallel, multi-center, single-blind study, comparing BLI-800 to an FDA approved bowel preparation in adult subjects undergoing colonoscopy.

Conditions Studied

Interventions

  • DRUG BLI-800
  • DRUG Polyethylene glycol 3350 based bowel preparation

Study Locations (11)

Florida

  • — Jupiter
  • — Miami
  • — New Smyrna Beach

Alabama

  • — Mobile

District of Columbia

  • — Washington D.C.

Louisiana

  • — Monroe

Maryland

  • — Laurel

New York

  • — Great Neck

North Carolina

  • — Raleigh

Pennsylvania

  • — Lancaster

Trial Details

FieldValue
Enrollment Target 400 participants
Start Date 2007-07
Est. Completion 2007-11
Phase Phase 3

Sponsor

Braintree Laboratories

10 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00503607

The ClinicalTrials.gov registry entry for NCT00503607 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 400 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Braintree Laboratories, which has 10 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Colonoscopy appearing as the primary indexed condition, and to 2 interventions — of which BLI-800 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00503607 reports 11 study locations spanning 9 distinct geographic areas — top geographies include Florida, Alabama, District of Columbia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00503607 about?

NCT00503607 is a clinical study titled "BLI-800-301: BLI-800 vs an Active Control Bowel Preparation in Adult Subjects Undergoing Colonoscopy". This is a randomized, parallel, multi-center, single-blind study, comparing BLI-800 to an FDA approved bowel preparation in adult subjects undergoing colonoscopy.

What is the current status of trial NCT00503607?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 400 participants. The study started on 2007-07. Estimated completion is 2007-11.

What conditions does trial NCT00503607 study?

This clinical trial studies the following conditions: Colonoscopy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00503607?

The interventions under investigation include: BLI-800 (DRUG), Polyethylene glycol 3350 based bowel preparation (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00503607?

This trial is sponsored by Braintree Laboratories, which has 10 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00503607 being conducted?

This trial has 11 study locations across Alabama, District of Columbia, Florida, Louisiana, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial