Abdominal Binder Study to Decrease Postoperative Pain

ClinicalTrials.gov ID: NCT01685593

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Official title

A Controlled Randomized Trial Examining the Ability of the Mott Compression Bonder to Decrease Postoperative Pain in Gynecologic Abdominal Laparotomy Patients.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

We conducted a controlled randomized trial examining the ability of the Mott abdominal Compression Binder to decrease postoperative pain in gynecologic abdominal laparotomy patients

Study identification

NCT ID: NCT01685593
Recruitment status: Completed
Study type: Interventional
Phase: Not applicable
Lead sponsor: Brooke Army Medical Center; Federal
Enrollment: 76 participants

Conditions and interventions

Conditions

Postoperative Pain

Interventions

abdominal binder Device
no binder Other

Device · Other

Eligibility (public fields only)

Age range: 18 Years and older
Sex: Female
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Jan 2001 (Type not available)
Primary completion: Feb 2006 (Actual)
Completion: Feb 2006 (Actual)
Last update posted: Sep 14, 2012

2001 – 2006

United States locations

U.S. sites: 1
U.S. states: 1
U.S. cities: 1

Facility	City	State	ZIP	Site status
Brooke Army Medical Center	Fort Sam Houston	Texas	78232	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT01685593, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Sep 14, 2012 · Synced Nov 13, 2026