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NCT00153127 · ClinicalTrials.gov registry record · Phase 4

Comparison of PolyethyleneGlycol and Placebo for Relief of Constipation From Constipating Medications

A Phase 4 study of Constipation, sponsored by Braintree Laboratories.

Completed
Registry status
Phase 4
Development phase
100
Enrollment target
4
Study locations

NCT00153127: Completed Phase 4 study of Constipation, sponsored by Braintree Laboratories.

NCT00153127 is a Phase 4 study of Constipation that has completed, run by Braintree Laboratories. The registered enrollment target is 100 participants, below the 204-participant average among 54 other Constipation trials with a reported enrollment target (51% lower). The trial reports 4 study locations across 4 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00153127, a Phase 4 study of Constipation, has completed, sponsored by Braintree Laboratories.

COMPLETED
Registry status
Phase 4
Development phase
100 participants
Enrollment target
4
Study locations

Study Summary

The purpose of this study is to assess treatment responses comparing a newly FDA-approved PEG laxative versus placebo.

Conditions Studied

Interventions

  • DRUG polyethyleneglycol3350

Study Locations (4)

Alabama

  • - Mobile

Florida

  • - St. Petersburg

Missouri

  • - St Louis

North Carolina

  • - Raleigh

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2001-11
Phase Phase 4
Braintree Laboratories

49 total trials

What the finished NCT00153127 record still lists

NCT00153127 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 204-participant average among 54 other Constipation trials with a reported enrollment target (51% lower).

The record links to 1 condition, with Constipation appearing as the primary indexed condition, and to 1 intervention - of which polyethyleneglycol3350 is the first listed.

NCT00153127 reports a single indexed study location in Alabama, Florida, Missouri.

Frequently Asked Questions

What is clinical trial NCT00153127 about?

NCT00153127 is a clinical study titled "Comparison of PolyethyleneGlycol and Placebo for Relief of Constipation From Constipating Medications". The purpose of this study is to assess treatment responses comparing a newly FDA-approved PEG laxative versus placebo.

What is the current status of trial NCT00153127?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2001-11.

What conditions does trial NCT00153127 study?

This clinical trial studies the following conditions: Constipation.

What interventions are being tested in trial NCT00153127?

The interventions under investigation include: polyethyleneglycol3350 (DRUG).

Who is sponsoring clinical trial NCT00153127?

This trial is sponsored by Braintree Laboratories, which has 49 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00153127 being conducted?

This trial has 4 study locations across Alabama, Florida, Missouri, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Constipation

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 NCT00153127's enrollment target sits among peer trials

100 17th of 54 higher than 35 of 54 other Constipation trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Constipation 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 NCT00153127, the US trial registry maintained by the National Library of Medicine. NCT00153127 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.