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

Tracking Information

First Received Date ^ICMJE

December 21, 2007

Last Updated Date

December 21, 2007

Start Date ^ICMJE

January 2004

Primary Completion Date

July 2007 (final data collection date for primary outcome measure)

Current Primary Outcome Measures ^ICMJE

Clinical and radiological outcome as assessed by closed-configuration MR defecography [ Designated as safety issue: No ]

Original Primary Outcome Measures ^ICMJE

Same as current

Change History

No Changes Posted

Current Secondary Outcome Measures ^ICMJE

Morbidity and Mortality after STARR [ Designated as safety issue: No ]

Original Secondary Outcome Measures ^ICMJE

Same as current

Descriptive Information

Brief Title ^ICMJE

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

Official Title ^ICMJE

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

Brief Summary

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

Detailed Description

Study Phase

Study Type ^ICMJE

Observational

Study Design ^ICMJE

Cohort, Prospective

Condition ^ICMJE

Obstructed Defecation Syndrome (ODS)

Intervention ^ICMJE

Study Arms / Comparison Groups

Publications *

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information

Recruitment Status ^ICMJE

Completed

Enrollment ^ICMJE

Completion Date

August 2007

Primary Completion Date

July 2007 (final data collection date for primary outcome measure)

Eligibility Criteria ^ICMJE

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

Gender

Both

Ages

18 Years to 90 Years

Accepts Healthy Volunteers

Contacts ^ICMJE

Contact information is only displayed when the study is recruiting subjects

Location Countries ^ICMJE

Switzerland

Administrative Information

NCT ID ^ICMJE

NCT00587080

Responsible Party

Daniel Dindo, MD, University Hospital Zurich

Study ID Numbers ^ICMJE

StV 33-2006

Study Sponsor ^ICMJE

University of Zurich

Collaborators ^ICMJE

Investigators ^ICMJE

Principal Investigator:

Daniel Dindo, MD

University of Zurich

Information Provided By

University of Zurich

Verification Date

December 2007

^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP