Evaluation of Efficacy, Safety and Tolerability of VeraCept IUS
Public ClinicalTrials.gov record NCT03633799. 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 Phase 3, Prospective, Multi-Center, Single-Arm, Open-Label Study to Evaluate VeraCept®, a Long-Acting Reversible Intrauterine Contraceptive for Contraceptive Efficacy, Safety, and Tolerability
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
To assess the contraceptive efficacy (prevention of pregnancy) of VeraCept
Study identification
- NCT ID
- NCT03633799
- Recruitment status
- Active, not recruiting
- Study type
- Interventional
- Phase
- Phase 3
- Enrollment
- 1,620 participants
Conditions and interventions
Conditions
Eligibility (public fields only)
- Age range
- Up to 45 Years
- Sex
- Female
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Aug 22, 2018 (Actual)
- Primary completion
- Sep 22, 2022 (Actual)
- Completion
- Sep 22, 2027 (Estimated)
- Last update posted
- Aug 22, 2025
2018 – 2027
United States locations
- U.S. sites
- 41
- U.S. states
- 24
- U.S. cities
- 36
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| MomDoc Women's Health Research | Scottsdale | Arizona | 85251 | — |
| Copperstate OB/GYN Associates | Tucson | Arizona | 85712 | — |
| Essential Access Health | Berkeley | California | 94710 | — |
| Essential Access Health | Los Angeles | California | 90010 | — |
| Empire Clinical Research | Pomona | California | 91767 | — |
| University of California, Davis Health System | Sacramento | California | 95817 | — |
| M3 Wake Research (formerly Women's Health Care Research) | San Diego | California | 92111 | — |
| M3 Wake Research (formerly Medical Center for Clinical Research) | San Diego | California | 92120 | — |
| Stanford University, Medical Center, Obstetrics and Gynecolocy | Stanford | California | 94305 | — |
| Velocity Clinical Research (formerly Downtown Women's Health Care) | Englewood | Colorado | 80110 | — |
| Altus Research, Inc | Lake Worth | Florida | 33461 | — |
| Emory University School of Medicine | Atlanta | Georgia | 30308 | — |
| Soapstone Center for Clinical Research | Decatur | Georgia | 30034 | — |
| Clinical Research Prime | Idaho Falls | Idaho | 83404 | — |
| Women's Health Advantage | Fort Wayne | Indiana | 46825 | — |
| Indiana University | Indianapolis | Indiana | 46202 | — |
| Praetorian Pharmaceutical Research | Marrero | Louisiana | 70072 | — |
| University of Michigan Von Voigtlander Women's Hospital | Ann Arbor | Michigan | 48109 | — |
| Planned Parenthood North Central States - Minneapolis | Minneapolis | Minnesota | 55408 | — |
| Planned Parenthood Great Rivers (formerly Planned Parenthood of the St. Louis Region and Southwest Missouri) | Manchester | Missouri | 63088 | — |
| Rex Garn Mabey Jr., MD | Las Vegas | Nevada | 89128 | — |
| Capital Health Lawrence OBGYN Research (formerly Lawrence OB/Gyn Clinical Research) | Lawrenceville | New Jersey | 08648 | — |
| Columbia University Medical Center, Division of Family Planning | New York | New York | 10032 | — |
| Duke University Medical Center | Durham | North Carolina | 27710 | — |
| University of Cincinnati/Reproductive Medicine Research | Cincinnati | Ohio | 45267 | — |
| The Ohio State University Ob/Gyn Research Office | Columbus | Ohio | 43210 | — |
| OHSU Women's Health Research Unit | Portland | Oregon | 97239 | — |
| University of Pennsylvania/Penn Family Planning and Pregnancy Loss Center | Philadelphia | Pennsylvania | 19104 | — |
| Clinical Research of Philadelphia | Philadelphia | Pennsylvania | 19114 | — |
| Magee-Womens Hospital, Center for Family Planning Research | Pittsburgh | Pennsylvania | 15213 | — |
| Medical Research South, LLC | Charleston | South Carolina | 29407 | — |
| Chattanooga Medical Research | Chattanooga | Tennessee | 37404 | — |
| The Jackson Clinic, PA | Jackson | Tennessee | 38305 | — |
| Advanced Research Associates | Corpus Christi | Texas | 78414 | — |
| Advances In Health | Pearland | Texas | 77584 | — |
| Wasatch Clinical Research | Salt Lake City | Utah | 84107 | — |
| University of Utah Healthcare Health Sciences Center | Salt Lake City | Utah | 84132 | — |
| Tidewater Physicians for Women | Norfolk | Virginia | 23502 | — |
| Eastern Virginia Medical | Norfolk | Virginia | 23507 | — |
| Seattle Clinical REsearch Center (formerly Seattle Women's Health) | Seattle | Washington | 98104 | — |
| University of Washington Medical Center | Seattle | Washington | 98117 | — |
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 NCT03633799, 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 Aug 22, 2025 · Synced Oct 21, 2026
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Open the official record
The complete public registry record, listed eligibility criteria, and available contact information for NCT03633799 live on ClinicalTrials.gov.