Microwave Ablation of Uterine Fibroids

NCT07780019 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2026-08-21

No results posted yet for this study

Summary

This prospective observational study aims to evaluate the effectiveness and acceptability of percutaneous or vaginal ultrasound guided microwave ablation for the treatment or symptomatic uterine fibroids. We will include 100 women.

Conditions

  • Uterine Fibroids (Leiomyoma)

Interventions

PROCEDURE

microwave ablation

ultrasound guided percutaneus microwave ablation

Sponsors & Collaborators

  • Turku University Hospital

    lead OTHER_GOV

Principal Investigators

  • Kirsi Joronen · Turku University Hospital

Eligibility

Min Age
18 Years
Max Age
56 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-05-01
Primary Completion
2031-12-31
Completion
2034-12-31

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07780019 on ClinicalTrials.gov