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Ascertaining Longterm Outcomes of Fibroid Treatments
Sponsor: Henry Ford Health System
Summary
The goal of the ALOFT study is to understand the health of women in the 12 years following a uterine fibroid (UF) treatment. ALOFT is a multi-center, prospective, observational cohort study of approximately 700 women who have undergone uterine-sparing treatment procedures for UF and previously participated in the longitudinal studies COMPARE-UF (NCT02260752) or ULTRA (NCT02100904). The primary uterine sparing treatment procedures undergone by study participants are myomectomy, endometrial ablation (EA), uterine artery embolization (UAE) and laparoscopic radiofrequency ablation (RFA). A smaller number of women may be studied who underwent focused ultrasound, intrauterine device (IUD), and medical management. Two follow-up study contacts with COMPARE-UF and ULTRA participants will occur to assess changes in UF symptoms and treatment failure which is defined as the need for another UF treatment procedure. Questionnaires will be used to collect data on patient-reported characteristics and outcomes and quality of life. The study's analyses will focus on comparisons of primary and secondary outcomes among women.
Official title: Long Term Effectiveness of Uterine Sparing Fibroid Treatments
Key Details
Gender
FEMALE
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
700
Start Date
2024-05-20
Completion Date
2027-08
Last Updated
2025-05-14
Healthy Volunteers
No
Conditions
Interventions
NA- no intervention
NA- no intervention
Locations (4)
University of California San Francisco
San Francisco, California, United States
Henry Ford Health
Detroit, Michigan, United States
Mayo Clinic
Rochester, Minnesota, United States
The University of North Carolina at Chapel Hill
Chapel Hill, North Carolina, United States