Stapled TransAnal Rectal Resection (STARR): Clinical and Radiological Outcome

December 21, 2007 updated by: University of Zurich

Stapled TransAnal Rectal Resection (STARR): Correlation Between Clinical and Radiological Outcome

To evaluate the correlation between clinical and radiological outcome after Stapled TransAnal Rectal Resection (STARR)

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

24

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Switzerland
      • Zurich, Switzerland, 8091
        • University Hospital, Clinic for Visceral and Transplantation Surgery

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 90 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Study Population

Patients with ODS and diagnosis of rectal redundancy (intussusception/rectoceles) in MR defecography

Description

Inclusion Criteria:

  • > 18 years
  • clinical signs of ODS with prior not effective conservative treatment
  • anterior rectoceles and/or intussusceptions in MR-defecography

Exclusion Criteria:

  • < 18 years
  • fixed enteroceles
  • severe fecal incontinence
  • external rectal prolapse
  • anismus

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Clinical and radiological outcome as assessed by closed-configuration MR defecography

Secondary Outcome Measures

Outcome Measure
Morbidity and Mortality after STARR

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of Zurich

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2004

Primary Completion (ACTUAL)

July 1, 2007

Study Completion (ACTUAL)

August 1, 2007

Study Registration Dates

First Submitted

December 21, 2007

First Submitted That Met QC Criteria

December 21, 2007

First Posted (ESTIMATE)

January 7, 2008

Study Record Updates

Last Update Posted (ESTIMATE)

January 7, 2008

Last Update Submitted That Met QC Criteria

December 21, 2007

Last Verified

December 1, 2007

More Information

Terms related to this study

Other Study ID Numbers

  • StV 33-2006

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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