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Treatment Outcomes of Vaginal Prolapse Repair

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00679276
First Posted: May 16, 2008
Last Update Posted: June 7, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
William Beaumont Hospitals
  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

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes 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:

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00679276


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

Responsible Party: Predeep Nagaraju, MD, William Beaumont Hospital
ClinicalTrials.gov Identifier: NCT00679276     History of Changes
Other Study ID Numbers: 2008-102
First Submitted: May 14, 2008
First Posted: May 16, 2008
Last Update Posted: June 7, 2010
Last Verified: June 2010

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