Prospective, multi-center, international, unblinded, single-arm trial of subjects undergoing FemBloc followed by ultrasound confirmation test.
Prospective, multi-center, international, unblinded, single-arm trial of subjects undergoing FemBloc followed by ultrasound confirmation test.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
573
Treatment for women who desire non-surgical permanent birth control by occlusion of the fallopian tubes.
New Horizons Clinical Trials
Chandler, Arizona, United States
RECRUITINGStanford University
Palo Alto, California, United States
RECRUITINGPregnancy Rate
Number of subjects who were told to rely on FemBloc for birth control and became pregnant through one (1) year.
Time frame: one (1) year
Reliance Rate
Number of subjects who were told to rely on FemBloc.
Time frame: ninety (90) days post treatment
Long term Pregnancy Rate
Number of subjects who were told to rely on FemBloc for birth control that became pregnant after one (1) year through 2-, 3-, 4-, and 5-years.
Time frame: Five (5) years
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University of California Davis
Sacramento, California, United States
RECRUITINGMidtown OB GYN North
Columbus, Georgia, United States
RECRUITINGRosemark WomenCare Specialists
Idaho Falls, Idaho, United States
RECRUITINGMaimonides Medical Center
Brooklyn, New York, United States
RECRUITINGColumbia University Medical Center
New York, New York, United States
RECRUITINGSeven Hills Women's Health Centers
Cincinnati, Ohio, United States
RECRUITINGChattanooga Medical Research LLC
Chattanooga, Tennessee, United States
RECRUITINGUniversity of Utah
Salt Lake City, Utah, United States
RECRUITING