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Abdominal Binder Study to Decrease Postoperative Pain

NCT ID: NCT01685593

Last Updated: 2012-09-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

76 participants

Study Classification

INTERVENTIONAL

Study Start Date

2001-01-31

Study Completion Date

2006-02-28

Brief Summary

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

Detailed Description

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Conditions

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Postoperative Pain

Keywords

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abdominal binder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Investigators

Study Groups

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regular bandage

no abdominal binder

Group Type SHAM_COMPARATOR

no binder

Intervention Type OTHER

abdominal binder

binder

Group Type EXPERIMENTAL

abdominal binder

Intervention Type DEVICE

Interventions

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abdominal binder

Intervention Type DEVICE

no binder

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* gynecologic abdominal laparotomy patients

Exclusion Criteria

* non gynecologic abdominal laparotomy patients
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Brooke Army Medical Center

FED

Sponsor Role lead

Responsible Party

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Edward R. Kost, M.D.

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Brooke Army Medical Center

Fort Sam Houston, Texas, United States

Site Status

Countries

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United States

Other Identifiers

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C.2001.128

Identifier Type: -

Identifier Source: org_study_id