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NCT00944736 · ClinicalTrials.gov registry record · Phase 3

Effect of VSL#3 on Intestinal Permeability in Pediatric Crohn's Disease

A Phase 3 study of Crohn's Disease, sponsored by Children's Mercy Hospital Kansas City.

Completed
Registry status
Phase 3
Development phase
12
Enrollment target
1
Study location

NCT00944736: Completed Phase 3 study of Crohn's Disease, sponsored by Children's Mercy Hospital Kansas City.

NCT00944736 is a Phase 3 study of Crohn's Disease that has completed, run by Children's Mercy Hospital Kansas City. The registered enrollment target is 12 participants, below the 2,394-participant average among 105 other Crohn's Disease trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00944736, a Phase 3 study of Crohn's Disease, has completed, sponsored by Children's Mercy Hospital Kansas City.

COMPLETED
Registry status
Phase 3
Development phase
12 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine the effect of a probiotic formulation, VSL#3, on intestinal permeability in pediatric patients with Crohn's disease.

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT Placebo
  • DIETARY_SUPPLEMENT VSL#3

Study Locations (1)

Missouri

  • The Children's Mercy Hospital - Kansas City

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2009-07
Est. Completion 2013-07
Phase Phase 3

What the finished NCT00944736 record still lists

NCT00944736 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 2,394-participant average among 105 other Crohn's Disease trials with a reported enrollment target (99% lower).

The record links to 1 condition, with Crohn's Disease appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT00944736 reports a single indexed study location in Missouri.

Frequently Asked Questions

What is clinical trial NCT00944736 about?

NCT00944736 is a clinical study titled "Effect of VSL#3 on Intestinal Permeability in Pediatric Crohn's Disease". The purpose of this study is to determine the effect of a probiotic formulation, VSL#3, on intestinal permeability in pediatric patients with Crohn's disease.

What is the current status of trial NCT00944736?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 12 participants. The study started on 2009-07. Estimated completion is 2013-07.

What conditions does trial NCT00944736 study?

This clinical trial studies the following conditions: Crohn's Disease.

What interventions are being tested in trial NCT00944736?

The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), VSL#3 (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT00944736?

This trial is sponsored by Children's Mercy Hospital Kansas City, which has 184 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00944736 being conducted?

This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Crohn's Disease

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00944736's enrollment target sits among peer trials

12 103rd of 105 higher than 2 of 105 other Crohn's Disease trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Crohn's Disease trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00944736, the US trial registry maintained by the National Library of Medicine. NCT00944736 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.