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NCT01626040 · ClinicalTrials.gov registry record

Evaluation of One-day Polyethylene Glycol Powder Solution for Colonoscopy in Children

A clinical trial, sponsored by Children's Hospital of Philadelphia.

Completed
Registry status
178
Enrollment target

NCT01626040: Completed study, sponsored by Children's Hospital of Philadelphia.

NCT01626040 is a clinical trial that has completed, run by Children's Hospital of Philadelphia. The registered enrollment target is 178 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01626040 has completed, sponsored by Children's Hospital of Philadelphia.

COMPLETED
Registry status
178 participants
Enrollment target

Study Summary

The purpose of this study is to examine the effects of current standard of care Polyethylene Gylcol powder (PEG-P)colonoscopy preparation on a patient's serum electrolytes, tolerance of the prep, and how well the bowel is cleansed. The primary aim is to determine the proportion of patients with clinically significant serum electrolyte abnormalities at the time of colonoscopy and how well the prep is tolerated. Secondary objectives include: 1) how well the bowel is cleansed with this preparation, and 2) to determine the most effective way to communicate instructions about the bowel preparation with the child and family.

Primary Outcome

the proportion of patients with clinically significant serum electrolyte abnormalities at the time of colonoscopy

Interventions

  • DRUG polyethylene glycol powder

Trial Details

FieldValue
Enrollment Target 178 participants
Start Date 2012-06
Est. Completion 2014-01
Children's Hospital of Philadelphia

431 total trials

What the finished NCT01626040 record still lists

NCT01626040 is an observational study that tracks outcomes without assigning an intervention. The registered 178 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 1 intervention - of which polyethylene glycol powder is the first listed.

NCT01626040 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01626040 about?

NCT01626040 is a clinical study titled "Evaluation of One-day Polyethylene Glycol Powder Solution for Colonoscopy in Children". The purpose of this study is to examine the effects of current standard of care Polyethylene Gylcol powder (PEG-P)colonoscopy preparation on a patient's serum electrolytes, tolerance of the prep, and how well the bowel is cleansed. The primary aim is to determine the proportion of patients with clin...

What is the current status of trial NCT01626040?

This trial is currently completed. The enrollment target is 178 participants. The study started on 2012-06. Estimated completion is 2014-01.

What interventions are being tested in trial NCT01626040?

The interventions under investigation include: polyethylene glycol powder (DRUG).

Who is sponsoring clinical trial NCT01626040?

This trial is sponsored by Children's Hospital of Philadelphia, which has 431 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT01626040, the US trial registry maintained by the National Library of Medicine. NCT01626040 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.