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

Obstructed Defecation Syndrome (ODS) Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00587080
• Other study ID #: StV 33-2006
• Status: Completed
• Phase: N/A
• First received: December 21, 2007
• Last updated: December 21, 2007
• Start date: January 2004
• Est. completion date: August 2007

Study information

• Verified date: December 2007
• Source: University of Zurich
• Contact: n/a
• Is FDA regulated: No
• Health authority: Switzerland: Federal Office of Public Health
• Study type: Observational

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: August 2007
• Est. primary completion date: July 2007
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 90 Years

Eligibility

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 Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Obstructed Defecation Syndrome (ODS)

Locations

Country	Name	City	State
Switzerland	University Hospital, Clinic for Visceral and Transplantation Surgery	Zurich

Sponsors (1)

Lead Sponsor	Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical and radiological outcome as assessed by closed-configuration MR defecography			No
Secondary	Morbidity and Mortality after STARR			No