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Recovery After Robotic Urogynecological Surgery: The Patient's Perspective

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00757432
First Posted: September 23, 2008
Last Update Posted: April 11, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University of Rochester
September 19, 2008
September 23, 2008
April 11, 2011
September 2007
September 2008   (Final data collection date for primary outcome measure)
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Complete list of historical versions of study NCT00757432 on ClinicalTrials.gov Archive Site
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Recovery After Robotic Urogynecological Surgery: The Patient's Perspective
Recovery After Robotic Urogynecological Surgery: The Patient's Perspective
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.
Not Provided
Observational
Observational Model: Cohort
Time Perspective: Retrospective
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Non-Probability Sample
Women who underwent DaVinci-assisted laparoscopic surgery
Urogynecology
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
22
September 2008
September 2008   (Final data collection date for primary outcome measure)

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
Sexes Eligible for Study: Female
21 Years and older   (Adult, Senior)
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00757432
25638
No
Not Provided
Not Provided
Gunhilde Buchsbaum, MD, University of Rochester
University of Rochester
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Principal Investigator: Gunhilde Buchsbaum, MD University of Rochester
University of Rochester
April 2011