Recovery After Robotic Urogynecological Surgery: The Patient's Perspective

Urogynecology Clinical Trial

Official title:

Recovery After Robotic Urogynecological Surgery: The Patient's Perspective

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00757432
• Other study ID #: 25638
• Status: Completed
• Phase: N/A
• First received: September 19, 2008
• Last updated: April 8, 2011
• Start date: September 2007
• Est. completion date: September 2008

Study information

• Verified date: April 2011
• Source: University of Rochester
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

The purpose of the study is to describe the patient experience, including pain scores, use of pain medications, resumption of usual activities, and bowel function in the post-operative period following robotic urogynecologic surgery. Additionally, to describe peri-operative parameters of robot-assisted urogynecologic surgery.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 22
• Est. completion date: September 2008
• Est. primary completion date: September 2008
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

• Women who underwent DaVinci-assisted laparoscopic surgery

• Completion of a post-operative quality assurance questionnaire from 09/2007 - 09/2008

Exclusion Criteria:

• Any women not meeting above inclusion criteria

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Urogynecology

Locations

Country	Name	City	State
United States	University of Rochester	Rochester	New York

Sponsors (1)

Lead Sponsor	Collaborator
University of Rochester

Country where clinical trial is conducted

United States,