Zestra in Women With Mixed Sexual Dysfunction
Public ClinicalTrials.gov record NCT00118495. 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
A Randomized, Placebo-Controlled, Double-Blind, Parallel Design Trial of the Efficacy and Safety of Zestra(TM) in Women With Mixed Desire/Interest/Arousal/Orgasm Disorders
Study identification
- NCT ID
- NCT00118495
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 3
- Lead sponsor
- QualiLife Pharmaceuticals
- Industry
- Enrollment
- 200 participants
Conditions and interventions
Conditions
Interventions
- Non-prescription Zestra(TM): patented formulation Drug
Drug
Eligibility (public fields only)
- Age range
- 21 Years to 65 Years
- Sex
- Female
- 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
- Feb 28, 2006
- Primary completion
- Not listed
- Completion
- Feb 28, 2007
- Last update posted
- Jul 5, 2007
2006 – 2007
United States locations
- U.S. sites
- 13
- U.S. states
- 10
- U.S. cities
- 13
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| West Coast Clinical Research | Tarzana | California | 91356 | — |
| Urology Research Options | Aurora | Colorado | 80012 | — |
| South Florida Medical Research | Aventura | Florida | 33180 | — |
| Center for Marital and Sexual Health of South Florida | West Palm Beach | Florida | 33401 | — |
| Northeast Indiana Research | Fort Wayne | Indiana | 46825 | — |
| Outpatient Clinical Research Facility | Indianapolis | Indiana | 46206-5250 | — |
| Lahey Clinic | Peabody | Massachusetts | 01960 | — |
| Accumed Research Associates | Garden City | New York | 11530 | — |
| Hudson Valley Urology, PC | Poughkeepsie | New York | 12601 | — |
| MetroHealth Medical Center | Cleveland | Ohio | 44109 | — |
| The Pelvic and Sexual Health Institute | Philadelphia | Pennsylvania | 19146 | — |
| Urology San Antonio Research, PA | San Antonio | Texas | 78229 | — |
| Midwest Research Specialists, LLC | Milwaukee | Wisconsin | 53209 | — |
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 NCT00118495, 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 Jul 5, 2007 · Synced Jul 21, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00118495 live on ClinicalTrials.gov.