Uterine Fibroid Research Database
Florida legislation establishing a uterine fibroid research database to collect patient data and support medical research on a condition affecting millions of women.
Florida legislation establishing a uterine fibroid research database to collect patient data and support medical research on a condition affecting millions of women.
SB 1728 would establish a uterine fibroid research database in Florida to collect and analyze data on the prevalence, diagnosis, treatment outcomes, and demographic patterns of uterine fibroids. The database would serve as a resource for researchers, healthcare providers, and public health officials to better understand this common condition that disproportionately affects women, particularly Black women.
Uterine fibroids affect approximately 26 million women of reproductive age in the U.S., yet remain understudied relative to their prevalence and impact on quality of life, fertility, and healthcare costs. A comprehensive state database could identify treatment disparities, improve clinical outcomes, and support research into prevention and more effective management strategies—particularly for populations experiencing higher incidence rates.
Compiled from official sources — confirm details with the bill’s official record.
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