Recovery After Robotic Urogynecological Surgery: The Patient's Perspective

This study has been completed.
Sponsor:
Information provided by:
University of Rochester
ClinicalTrials.gov Identifier:
NCT00757432
First received: September 19, 2008
Last updated: April 8, 2011
Last verified: April 2011
  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

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

Further study details as provided by University of Rochester:

Enrollment: 22
Study Start Date: September 2007
Study Completion Date: September 2008
Primary Completion Date: September 2008 (Final data collection date for primary outcome measure)
  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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

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: Gunhilde Buchsbaum, MD, University of Rochester
ClinicalTrials.gov Identifier: NCT00757432     History of Changes
Other Study ID Numbers: 25638
Study First Received: September 19, 2008
Last Updated: April 8, 2011
Health Authority: United States: Institutional Review Board

ClinicalTrials.gov processed this record on September 14, 2014