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Pregnancy outcome after Hifu treatment uterus fibroids and comparison with surgery option

Pregnancy outcome after Hifu treatment uterus fibroids and comparison with surgery option - Pregnancy outcome

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00016769
Enrollment
300
Registered
2019-04-15
Start date
2015-04-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

D25

Interventions

Group 1: Pregnancy outcome patients with fibroids enrolled and performed HIFU treatment are monitored by telephone interviews and the results are noted Group 2: Pregnancy outcome patients with fibroid

Sponsors

Pro-Familia Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
22 Years to 43 Years

Inclusion criteria

Inclusion criteria: Presence of Symptomatic uterus fibroid ( heavy bleeding, pain, pelvic compression) in women with fertility and sterility disorder

Exclusion criteria

Exclusion criteria: Lack of approval, contraidicates in MRI environment

Design outcomes

Primary

MeasureTime frame
Fertility and pregnancy outcomes are monitored by telephone interviews and the results are noted

Secondary

MeasureTime frame
The Reduction of symptoms is evaluated by the regular gynaecological staff through examinations, blood tests, ultrasounds scans, and quality of life questionnaires.

Countries

Poland

Contacts

Public ContactTomasz Lozinski

Pro-Familia Hospital

tomloz@pro-familia.pl+48177735700

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026