Recovery After Robotic Urogynecological Surgery: The Patient's Perspective

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00757432

Enrollment

Registered

2008-09-23

Start date

2007-09-30

Completion date

2008-09-30

Last updated

2011-04-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urogynecology

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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

21 Years to No maximum

Healthy volunteers

Yes

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

Countries

United States

Outcome results