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Recovery After Robotic Urogynecological Surgery: The Patient's Perspective

NCT00757432 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 22

Last updated 2011-04-11

No results posted yet for this study

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.

Conditions

  • Urogynecology

Sponsors & Collaborators

  • University of Rochester

    lead OTHER

Principal Investigators

  • Gunhilde Buchsbaum, MD · University of Rochester

Eligibility

Min Age
21 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-09-30
Primary Completion
2008-09-30
Completion
2008-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00757432 on ClinicalTrials.gov