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Microwave Ablation for Leiomyoma (MYOMIC2)

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Karolinska Institute

Status

Enrolling

Conditions

Uterine Fibroid

Study type

Observational

Funder types

Other

Identifiers

NCT04240262
MYOMIC2

Details and patient eligibility

About

This prospective observational study aims to evaluate the effectiveness and acceptability of percutaneous or vaginal ultrasound guided microwave ablation for the treatment of symptoms related to uterine fibroids. We will include 200 women.

Enrollment

200 estimated patients

Sex

Female

Ages

25+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • premenopausal
  • no future child wish
  • acceptable risks for general anestesia or sedation
  • willing to comply with protocol

Exclusion criteria

  • current or future child wish
  • bleeding disorder with increased risk of bleeding

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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