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Treatment Outcomes of Vaginal Prolapse Repair

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ClinicalTrials.gov Identifier: NCT00679276
Recruitment Status : Completed
First Posted : May 16, 2008
Last Update Posted : June 7, 2010
Sponsor:
Information provided by:
William Beaumont Hospitals

Brief 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.

Condition or disease Intervention/treatment
Vaginal Prolapse Procedure: Prolift

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.

Study Type : Observational
Actual Enrollment : 291 participants
Observational Model: Case Control
Time Perspective: Retrospective
Official Title: Treatment Outcomes of Vaginal Prolapse Repair
Study Start Date : May 2008
Actual Primary Completion Date : May 2010
Actual Study Completion Date : May 2010

Group/Cohort Intervention/treatment
1
Patients having surgical repair of a vaginal prolapse .
Procedure: Prolift
surgical repair of vaginal prolapse





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


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

Responsible Party: Predeep Nagaraju, MD, William Beaumont Hospital
ClinicalTrials.gov Identifier: NCT00679276     History of Changes
Other Study ID Numbers: 2008-102
First Posted: May 16, 2008    Key Record Dates
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