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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00679276
Other study ID # 2008-102
Secondary ID
Status Completed
Phase N/A
First received May 14, 2008
Last updated June 4, 2010
Start date May 2008
Est. completion date May 2010

Study information

Verified date June 2010
Source William Beaumont Hospitals
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Chart review conducted on all patients having had Prolift surgery since 2005 by Dr. Lary Sirls, Dr. Predeep Nagaraju and Dr. Kenneth Peters at William Beaumont Hospital.


Description:

Chart review conducted on all patients having had Prolift surgery since 2005 by Dr. Lary Sirls, Dr. Predeep Nagaraju and Dr. Kenneth Peters at William Beaumont Hospital. Preoperative, intraoperative and post-operative data will be collected from the hospital and physician medical records. A questionnaire will be mailed to patients whose charts have been reviewed to assess urinary and bowel function, satisfaction with treatment and changes in sexual function. Completion of the questionnaire is voluntary.


Recruitment information / eligibility

Status Completed
Enrollment 291
Est. completion date May 2010
Est. primary completion date May 2010
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Women having Prolift repair at William Beaumont Hospital

Exclusion Criteria:

Study Design

Observational Model: Case Control, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Procedure:
Prolift
surgical repair of vaginal prolapse

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
William Beaumont Hospitals
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