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NCT02165436 · ClinicalTrials.gov registry record · NA

Chewing Gum Facilitates an Earlier Return to Bowel Function in Pediatric Scoliosis Patients: A Prospective Randomized Study

A NA study, sponsored by University of Alabama at Birmingham.

Completed
Registry status
NA
Development phase
83
Enrollment target

NCT02165436: Completed NA study, sponsored by University of Alabama at Birmingham.

NCT02165436 is a NA study that has completed, run by University of Alabama at Birmingham. The registered enrollment target is 83 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02165436, a NA study, has completed, sponsored by University of Alabama at Birmingham.

COMPLETED
Registry status
NA
Development phase
83 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the effectiveness of chewing gum on reducing post-operative ileus and reducing post-operative gastrointestinal symptoms in pediatric patients undergoing surgical correction of scoliosis. This study would provide minimal risk to its study population, and has the opportunity to provide a benefit to patients undergoing scoliosis surgery. If shown to be effective, this could lead to changes and improvement of the post-operative course for pediatric scoliosis patients.

Primary Outcome

Patients are interviewed daily as inpatient and then several days after surgery to determine the time (reported in hours post-operative) first flatus and first bowel movement was experienced.

Interventions

  • OTHER Control
  • OTHER Chewing gum

Trial Details

FieldValue
Enrollment Target 83 participants
Start Date 2009-07
Est. Completion 2013-07
Phase NA
University of Alabama at Birmingham

1,160 total trials

What the finished NCT02165436 record still lists

NCT02165436 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 83 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).

The record links to 0 conditions, and to 2 interventions - of which Control is the first listed.

NCT02165436 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02165436 about?

NCT02165436 is a clinical study titled "Chewing Gum Facilitates an Earlier Return to Bowel Function in Pediatric Scoliosis Patients: A Prospective Randomized Study". The purpose of this study is to evaluate the effectiveness of chewing gum on reducing post-operative ileus and reducing post-operative gastrointestinal symptoms in pediatric patients undergoing surgical correction of scoliosis. This study would provide minimal risk to its study population, and has t...

What is the current status of trial NCT02165436?

This trial is currently completed. It is a NA study. The enrollment target is 83 participants. The study started on 2009-07. Estimated completion is 2013-07.

What interventions are being tested in trial NCT02165436?

The interventions under investigation include: Control (OTHER), Chewing gum (OTHER).

Who is sponsoring clinical trial NCT02165436?

This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02165436's enrollment target sits among peer trials

83 990th of 2000 higher than 1,011 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT02165436, the US trial registry maintained by the National Library of Medicine. NCT02165436 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.