This is an open, post-marketing surveillance study obtaining data retrospectively on 300 women, of any age, treated with the BD-OTS for postpartum uterine bleeding.
Study Type
OBSERVATIONAL
Enrollment
300
Banner Good Samaritan Medical Center
Phoenix, Arizona, United States
Presbyterian/St. Luke's Medical Center
Denver, Colorado, United States
Orlando Health
Orlando, Florida, United States
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Monmouth Medical Center
Long Branch, New Jersey, United States
UHS - Wilson Medical Center
Johnson City, New York, United States
University of Cincinnati
Cincinnati, Ohio, United States
Toledo Hospital
Toledo, Ohio, United States
Medical University of South Carolina
Charleston, South Carolina, United States
Erlanger
Chattanooga, Tennessee, United States
St. David's Medical Center
Austin, Texas, United States
...and 1 more locations