Safety and Efficacy Study of Oral Fispemifene for the Treatment of Sexual Dysfunction in Hypogonadal Men
Public ClinicalTrials.gov record NCT02443090. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
An 8-Week Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Oral Fispemifene for the Treatment of Sexual Dysfunction in Hypogonadal Men
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
To evaluate the safety and efficacy of fispemifene in men with secondary hypogonadism and sexual side effects.
Study identification
- NCT ID
- NCT02443090
- Recruitment status
- Not listed
- Study type
- Interventional
- Phase
- Phase 2
- Enrollment
- 160 participants
Conditions and interventions
Eligibility (public fields only)
- Age range
- 18 Years to 64 Years
- Sex
- Male
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Apr 30, 2015
- Primary completion
- Sep 30, 2015
- Completion
- Mar 31, 2016
- Last update posted
- Nov 12, 2015
2015 – 2016
United States locations
- U.S. sites
- 16
- U.S. states
- 9
- U.S. cities
- 15
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Baptist Health Center for Clinical Research | Little Rock | Arkansas | 72205 | — |
| San Diego Clinical Trials | San Diego | California | 92120 | — |
| Genesis Research LLC | San Diego | California | 92123 | — |
| Meridien Research | Bradenton | Florida | 34208 | — |
| Clinical Research of South Florida | Coral Gables | Florida | 33134 | — |
| Well Pharma Medical Research | Miami | Florida | 33144 | — |
| Regional Urology, LLC | Shreveport | Louisiana | 71106 | — |
| Premier Urology Associates, LLC, dba AdvanceMed Research | Lawrence | New Jersey | 08648 | — |
| The Urological Institute of Northeastern New York | Albany | New York | 12208 | — |
| AccuMed Research Associates | Garden City | New York | 11530 | — |
| Bruce R. GIlbert, MD, PhD, PC | Great Neck | New York | 11022 | — |
| Manhattan Medical Research Practice PLLC | New York | New York | 10016 | — |
| Volunteer Research | Knoxville | Tennessee | 37920 | — |
| Clinical Research Associates, Inc. | Nashville | Tennessee | 37203 | — |
| Physicians' Research Options LLC | Draper | Utah | 84020 | — |
| Clinical Research Associates of Tidewater, Inc. | Norfolk | Virginia | 23507 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT02443090, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Nov 12, 2015 · Synced Sep 11, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT02443090 live on ClinicalTrials.gov.