Clinical Trials Logo
  1. Home
  2. Female Sexual Dysfunction
  3. NCT03498443
  4. Details
NCT03498443 Clinical Trial

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

Female Sexual Dysfunction Clinical Trial

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

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03498443
Other study ID # Asamir
Secondary ID
Status Recruiting
Phase
First received April 8, 2018
Last updated April 8, 2018
Start date September 1, 2017
Est. completion date May 1, 2018

Study information
Verified date April 2018
Source Beni-Suef University
Contact ashraf samir, md
Phone 00201002526321
Email ashrafsamir81@yahoo.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

study on female sexual function after different prolapse surgeries

Recruitment information / eligibility
Status Recruiting
Enrollment 200
Est. completion date May 1, 2018
Est. primary completion date May 2018
Accepts healthy volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- sex active prolapse surgery

Exclusion Criteria:

- not sex active any psychiatric problem

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Egypt Benisuef Uneversity Hospital Bani Suwayf BeniSuef

Sponsors (1)
Lead Sponsor Collaborator
Beni-Suef University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary sexual function after prolapse surgeries questionnaire month3
See also
  Status Clinical Trial Phase
Completed NCT05806424 - Investigation of Awareness Levels of Women Living in Turkey About Kegel Exercises and Pelvic Floor Muscles
Completed NCT01364623 - PK Study of Testosterone Nasal Gel (TBS-2) in Healthy Premenopausal Women Phase 1
Completed NCT06060691 - the Ameliorating Effects of Antioxidant Gel on Female Arousal Disorder and Sexual Dysfunction Phase 1
Recruiting NCT04419961 - Sexual Dysfunction and an Educational Program to Improve the Quality of Sexual Function in Vietnamese Pregnant Women in First Trimester N/A
Completed NCT04122703 - Trial of Tibial Nerve Stimulation for Treating Sexual Dysfunction N/A
Completed NCT03232801 - A Mindfulness-based Intervention for Older Women With Low Sexual Desire N/A
Completed NCT04124640 - Observational Study in Real Life to Describe the Libicare® Effectiveness in Female Sexual Dysfunction.
Completed NCT00995072 - Comparative Effects of Nebivolol and Metoprolol on Female Sexual Function N/A
Active, not recruiting NCT05168371 - Cognitive-Behavioural & Mindfulness-Based Online Programs for Female Sexual Dysfunction N/A
Completed NCT04384172 - Effect of Peripheral Neuromodulation on Vaginal Blood Flow N/A
Recruiting NCT06237166 - Evaluation of an Online Intervention for Female Sexual Dysfunction N/A
Completed NCT03463707 - BP101 for Adults With Female Sexual Dysfunction Phase 3
Recruiting NCT01078077 - The Impact of a Topical Vasodilating Cream on Female Sexual Experience N/A
Completed NCT01724658 - Effectiveness of Testosterone Undecanoate to Improve Sexual Function in Postmenopausal Women Phase 2
Completed NCT02229721 - Effect of Chronic Intranasal Oxytocin Administration on Sexual Function in Pre- and Postmenopausal Women Phase 2
Completed NCT00479570 - Study To Investigate Effect Of A New Drug (PF-00446687) In Post-Menopausal Women Who Suffer From Sexual Dysfunction. Phase 2
Not yet recruiting NCT06116045 - Evaluation of the Efficacy, Safety and Tolerability of BZ371A in Women With Sexual Arousal Disorder Phase 2
Withdrawn NCT02862184 - Female Sexual Dysfunction, Risks and Outcomes (FSFI) N/A
Completed NCT01195701 - Clitoral Location in Relation to Sexual Function Using Pelvic Imaging N/A
Completed NCT04484753 - Validation of iPelvis App for Female Pelvic Floor Dysfunction N/A