Status:
TERMINATED
Evaluation of The Vaginal Renewal™ Program in Gynecologic Cancer Patients Experiencing Sexual Dysfunction
Lead Sponsor:
University of Wisconsin, Madison
Conditions:
Sexual Dysfunction, Physiological
Eligibility:
FEMALE
18+ years
Phase:
PHASE2
Brief Summary
This is a randomized controlled trial designed to evaluate the effect of the Vaginal Renewal™ Program (VRP), consisting of the use of a vibrating vaginal wand, manual massage and a water based lubrica...
Eligibility Criteria
Inclusion
- Age ≥18
- History of a gynecologic cancer
- No evidence of disease at time of inclusion in the study
- Postmenopausal (either surgical or natural menopause)
- Self report of sexual dysfunction that did not predate cancer diagnosis
- Suspected physical component to sexual dysfunction with the participant, not sexual partner
- Desire to improve sexual function
- ECOG Performance status score of 2 or better
- Six months or greater from last surgical and/or radiation treatment
Exclusion
- History of sexual reassignment
- Presence of vaginal fistula
- Does not desire to improve sexual function
- Already using the vaginal renewal program
- Not fluent in English
- Incarceration
Key Trial Info
Start Date :
August 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2013
Estimated Enrollment :
29 Patients enrolled
Trial Details
Trial ID
NCT01444911
Start Date
August 1 2011
End Date
May 1 2013
Last Update
December 9 2019
Active Locations (1)
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1
University of Wisconsin School of Medicine and Public Health Madison, Wisconsin, United States
Madison, Wisconsin, United States, 53792