Recovery After Robotic Urogynecological Surgery: The Patient's Perspective

This study has been completed.

First Received: September 19, 2008 Last Updated: September 22, 2008 History of Changes

Sponsored by:	University of Rochester
Information provided by:	University of Rochester
ClinicalTrials.gov Identifier:	NCT00757432

Purpose

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.

Condition
Urogynecology

MedlinePlus related topics: Surgery

U.S. FDA Resources

Study Type:	Observational
Study Design:	Cohort, Retrospective
Official Title:	Recovery After Robotic Urogynecological Surgery: The Patient's Perspective

Further study details as provided by University of Rochester:

Estimated Enrollment:	30
Study Start Date:	September 2008

Eligibility

Ages Eligible for Study:	21 Years and older
Genders Eligible for Study:	Female
Accepts Healthy Volunteers:	Yes
Sampling Method:	Non-Probability Sample

Study Population

Women who underwent DaVinci-assisted laparoscopic surgery

Criteria

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

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00757432

Locations

United States, New York
University of Rochester
Rochester, New York, United States, 14642

Sponsors and Collaborators

University of Rochester

Investigators

Principal Investigator:

Gunhilde Buchsbaum, MD

University of Rochester

More Information

No publications provided

Responsible Party:	University of Rochester ( Gunhilde Buchsbaum, MD )
Study ID Numbers:	25638
Study First Received:	September 19, 2008
Last Updated:	September 22, 2008
ClinicalTrials.gov Identifier:	NCT00757432 History of Changes
Health Authority:	United States: Institutional Review Board

ClinicalTrials.gov processed this record on May 07, 2009