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Uterine Fibroids (Leiomyoma)MyoMwaNCT07780019

Microwave Ablation of Uterine Fibroids

An observational study of Uterine Fibroids (Leiomyoma), run by Turku University Hospital at 1 site in Finland.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record

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Trial 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. Read more about this study

Who is it for?
Ages 18 to 56 years, women only
Conditions the study is for
Uterine Fibroids (Leiomyoma)
What is being tested?
microwave ablation
Type of treatment
Surgery or procedure
How many people
100 participants
Where
1 siteFinland
Study dates
1 May 2026to Dec 2034
How long will I take part?
12 Months
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 56 years
  • Women only
  • No healthy volunteers
  • Adult

Study population: patients undergoing mwa for symptomatic uterine fibroids will be recruited for this study

Who may be able to join

  • symptomatic fibroids
  • premenopausal status
  • acceptable risks for general anestesia or sedation
  • willing to undergo mwa treatment and participate in the study

Who cannot join

  • postmenopausal status
  • bleeding disorder with increased risk of bleeding

Trial locations and contacts

1 site in 1 country.

Finland1 site
  • Turku University Hospital

    Turku

Other trials in Finland

About this study

Official title: Prospective Observational Study of Microwave Ablation of Uterine Fibroids (MyoMwa)

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.

Being tested
microwave ablation
Keywords
microwave ablation
Medical subject headings
Leiomyoma

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • microwave ablationProcedure or surgery

    ultrasound guided percutaneus microwave ablation

Study groups in NCT07780019
Study groupRoleWhat they receive
patients with symptomatic uterine fibroidsPatients with symptomatic uterine fibroids, who will undergo microwave ablation of fibroids as a clinical treatment are recruited in this study.
Receives: Procedure: microwave ablation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Symptom severity of uterine fibroids and quality of life

    Score of validated form Uterine Fibroid symptom - Quality of life questinnaire. minimum 0, maximum 100 where higher scores indicate higher symptom severity

    Measured: 12 months

  2. suitability of mwa for general fibroid population

    objective and subjective outcome of mwa in different fibroid types, sizes and locations

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Aug 2026
  2. Study start1 May 2026
  3. Primary completionDec 2031 (estimated)
  4. Study completionDec 2034 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
100 participants (estimated)
Target duration
12 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT07780019
Sponsor's protocol ID
T2026/43353
Acronym
MyoMwa
Status last verified
Aug 2026
First submitted
12 Aug 2026
Last updated
21 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

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