What this study is
Prospective, multi-center, international, unblinded, single-arm trial of subjects undergoing FemBloc followed by ultrasound confirmation test.
What's being tested
- FemBloc
Intervention · DEVICE
Treatment for women who desire non-surgical permanent birth control by occlusion of the fallopian tubes.
Study details
- Official title
- FINALE: Prospective Multi-Center Trial for FemBloc INtratubal Occlusion for TranscervicAL PErmanent Birth Control
- Sponsor
- Femasys Inc.
- Conditions
- Contraception
- Enrolling
- 573 people
- Starts
- 2023-10-31
- Est. completion
- 2031-06
- Design
- Open-label, single group
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 21 Years – 50 YearsSex FEMALEHealthy volunteers AcceptedYou may qualify if
- Female, 21 - 50 years of age desiring permanent birth control.
- Sexually active with male partner.
- Regular menstrual cycle for last 3 months or on hormonal contraceptives.
You can't join if
- Uncertainty about the desire to end fertility.
- Known or suspected pregnancy.
- Prior tubal surgery, including sterilization attempt.
- Presence, suspicion, or previous history of gynecologic malignancy.
- Scheduled to undergo concomitant intrauterine procedures (i.e. endometrial ablation) at the time of either FemBloc Treatment or prior to final confirmation test.
- Abnormal uterine bleeding requiring evaluation or treatment.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (12)
12 openNew Horizons Clinical Trials
Chandler, Arizona, United States
- Research Coordinator · Contact480-496-2236sflores@womenshealthaz.com
RecruitingStanford University
Palo Alto, California, United States
- Research Coordinator · Contact650-497-5175mrodrig@stanford.edu
RecruitingUniversity of California Davis
Sacramento, California, United States
- Research Coordinator · Contact916-734-6846obgyncrcs@health.ucdavis.edu
RecruitingMidtown OB GYN North
Columbus, Georgia, United States
- Research Coordinator · Contact706-320-2547rebeccaw@midtownob.com
RecruitingAtrium Health Navicent
Macon, Georgia, United States
- Research Coordinator · Contact478-633-1522Jennifer.Crawford3@Advocatehealth.org
RecruitingRosemark WomenCare Specialists
Idaho Falls, Idaho, United States
- Research Coordinator · Contact208-557-2924nramirez@rosemark.net
RecruitingMaimonides Medical Center
Brooklyn, New York, United States
- Research Coordinator · Contact718-283-7962NRobins@maimo.org
RecruitingColumbia University Medical Center/NYPH
New York, New York, United States
- Research Coordinator · Contact212-305-9672na2678@cumc.columbia.edu
RecruitingSeven Hills Women's Health Centers
Cincinnati, Ohio, United States
- Research Coordinator · Contact513-290-3221btillman.shcrg@gmail.com
RecruitingChattanooga Medical Research LLC
Chattanooga, Tennessee, United States
- Research Coordinator · Contact423-648-7794cbryars@chattmedresearch.com
RecruitingBaylor Scott & White Research Institute
Temple, Texas, United States
- Research Coordinator · Contact254-724-7727Michelle.Vanecek@BSWHealth.org
RecruitingUniversity of Utah
Salt Lake City, Utah, United States
- Research Coordinator · Contact801-231-2774amy.orr@hsc.utah.edu
Recruiting
Study team
Sponsor
Femasys Inc.
Study ID CP-100-009
Study director
Study Sponsor
Medical Affairs and Clinical Development
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.