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The purpose of this study is to identify breast and gynecologic cancer patients with sexual dysfunction, to measure sexual dysfunction with the Female Sexual Function Index (FSFI) and to provide Patients with the opportunity during this six-month period to follow up with a healthcare provider to discuss the sexual dysfunction needs and to see if a medical intervention can be of aid.
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Interventional model
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20 participants in 1 patient group
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Central trial contact
Ayokunle Ogunye; Lavanya P Parsons, MD
Data sourced from clinicaltrials.gov
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