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Recovery After Robotic Urogynecological Surgery: The Patient's Perspective

Completed
Conditions
Urogynecology
Registration Number
NCT00757432
Lead Sponsor
University of Rochester
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
22
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

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Rochester

🇺🇸

Rochester, New York, United States

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