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Effect of Pelvic Organ Prolapse Surgeries on Female Sexual Function in Egyptian Women

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.
 
ClinicalTrials.gov Identifier: NCT03498443
Recruitment Status : Unknown
Verified April 2018 by Ashraf samir MD, Beni-Suef University.
Recruitment status was:  Recruiting
First Posted : April 13, 2018
Last Update Posted : April 13, 2018
Sponsor:
Information provided by (Responsible Party):
Ashraf samir MD, Beni-Suef University

Brief Summary:
study on female sexual function after different prolapse surgeries

Condition or disease
Female Sexual Dysfunction

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Study Type : Observational
Estimated Enrollment : 200 participants
Observational Model: Case-Control
Time Perspective: Prospective
Official Title: Effect of Pelvic Organ Prolapse Surgeries on Female Sexual Function in Egyptian Women
Actual Study Start Date : September 1, 2017
Estimated Primary Completion Date : May 2018
Estimated Study Completion Date : May 1, 2018

Resource links provided by the National Library of Medicine





Primary Outcome Measures :
  1. sexual function after prolapse surgeries [ Time Frame: month3 ]
    questionnaire



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Female
Sampling Method:   Probability Sample
Study Population
females e prolapse ser
Criteria

Inclusion Criteria:

  • sex active prolapse surgery

Exclusion Criteria:

  • not sex active any psychiatric problem

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): NCT03498443


Contacts
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Contact: ashraf samir, md 00201002526321 ashrafsamir81@yahoo.com

Locations
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Egypt
Benisuef Uneversity Hospital Recruiting
Banī Suwayf, BeniSuef, Egypt, 62511
Contact: ashraf samir, md         
Sponsors and Collaborators
Beni-Suef University

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Responsible Party: Ashraf samir MD, lecturer of obstetrics and gynecology BeniSuef university, Beni-Suef University
ClinicalTrials.gov Identifier: NCT03498443    
Other Study ID Numbers: Asamir
First Posted: April 13, 2018    Key Record Dates
Last Update Posted: April 13, 2018
Last Verified: April 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Prolapse
Pelvic Organ Prolapse
Pathological Conditions, Anatomical