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ENROLLING BY INVITATION
NCT06430320

Ascertaining Longterm Outcomes of Fibroid Treatments

Sponsor: Henry Ford Health System

View on ClinicalTrials.gov

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

OTHER

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