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Intraperitoneal Versus Extraperitoneal Colostomy

NCT ID: NCT00964379

Last Updated: 2013-11-13

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

PHASE3

Total Enrollment

81 participants

Study Classification

INTERVENTIONAL

Study Start Date

1988-01-31

Study Completion Date

2013-06-30

Brief Summary

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This is a prospective randomized trial of intraperitoneal versus extraperitoneal techniques for construction of terminal iliac fossa colostomies.

Detailed Description

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Conditions

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Colostomy

Keywords

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Intra versus extraperitoneal colostomy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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intraperitoneal colostomy

Group Type ACTIVE_COMPARATOR

intraperitoneal or extraperitoneal colostomy

Intervention Type PROCEDURE

creation of colostomy

extraperitoneal colostomy

Group Type ACTIVE_COMPARATOR

intraperitoneal or extraperitoneal colostomy

Intervention Type PROCEDURE

creation of colostomy

Interventions

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intraperitoneal or extraperitoneal colostomy

creation of colostomy

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* permanent colostomy

Exclusion Criteria

* none
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Mayo Clinic

OTHER

Sponsor Role lead

Responsible Party

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Mayo Clinic

Locations

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Mayo Clinic

Rochester, Minnesota, United States

Site Status

Countries

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United States

Other Identifiers

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528-93

Identifier Type: -

Identifier Source: org_study_id