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Treatment Outcomes of Vaginal Prolapse Repair

This study has been completed.
Sponsor:
Information provided by:
William Beaumont Hospitals
ClinicalTrials.gov Identifier:
NCT00679276
First received: May 14, 2008
Last updated: June 4, 2010
Last verified: June 2010
History of Changes
  Purpose

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.


Condition Intervention
Vaginal Prolapse
 Procedure: Prolift

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Retrospective
Official Title: Treatment Outcomes of Vaginal Prolapse Repair

Further study details as provided by William Beaumont Hospitals:

Enrollment: 291
Study Start Date: May 2008
Study Completion Date: May 2010
Primary Completion Date: May 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
1
Patients having surgical repair of a vaginal prolapse .
 Procedure: Prolift
surgical repair of vaginal prolapse

Detailed 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.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients having prolift surgery at William Beaumont Hospital by Dr. Lary Sirls, Dr. Predeep Nagaraju, and Dr. Kenneth Peters.

Criteria

Inclusion Criteria:

  • Women having Prolift repair at William Beaumont Hospital

Exclusion Criteria:

  • None
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00679276

Sponsors and Collaborators
William Beaumont Hospitals
Investigators
Principal Investigator: Predeep Nagaraju, MD William Beaumont Hospitals
  More Information

No publications provided

Responsible Party: Predeep Nagaraju, MD, William Beaumont Hospital
ClinicalTrials.gov Identifier: NCT00679276     History of Changes
Other Study ID Numbers: 2008-102
Study First Received: May 14, 2008
Last Updated: June 4, 2010
Health Authority: United States: Institutional Review Board

Keywords provided by William Beaumont Hospitals:
vaginal prolapse

Additional relevant MeSH terms:
Prolapse
Uterine Prolapse
Pathological Conditions, Anatomical
 Uterine Diseases
Genital Diseases, Female
Pelvic Organ Prolapse

ClinicalTrials.gov processed this record on May 23, 2013