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COMPLETED NA

Prevention of Ileus After Gynecologic Surgery Using Chewing Gum

NCT00831246 · View on ClinicalTrials.gov ↗

Study Summary

This study will attempt to determine if the use of chewing gum can cause the early return of bowel function after gynecologic surgery.

Conditions Studied

Interventions

  • OTHER chewing gum - Extra Winterfresh
  • OTHER Standard Post-Op Care

Study Locations (1)

Ohio

  • Aultman Health Foundation — Canton

Trial Details

FieldValue
Enrollment Target 400 participants
Start Date 2008-04
Est. Completion 2009-04
Phase NA

Sponsor

Aultman Health Foundation

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00831246

The ClinicalTrials.gov registry entry for NCT00831246 describes a study currently listed as completed. It is categorized as NA, 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 Aultman Health Foundation, which has 3 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 Ileus appearing as the primary indexed condition, and to 2 interventions — of which chewing gum - Extra Winterfresh 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: NCT00831246 reports 1 study location spanning 1 distinct geographic area — top geographies include Ohio. 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 NCT00831246 about?

NCT00831246 is a clinical study titled "Prevention of Ileus After Gynecologic Surgery Using Chewing Gum". This study will attempt to determine if the use of chewing gum can cause the early return of bowel function after gynecologic surgery.

What is the current status of trial NCT00831246?

This trial is currently completed. It is a NA study. The enrollment target is 400 participants. The study started on 2008-04. Estimated completion is 2009-04.

What conditions does trial NCT00831246 study?

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

What interventions are being tested in trial NCT00831246?

The interventions under investigation include: chewing gum - Extra Winterfresh (OTHER), Standard Post-Op Care (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00831246?

This trial is sponsored by Aultman Health Foundation, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00831246 being conducted?

This trial has 1 study location across Ohio. 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