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Effect of cabergoline in treatment of uterine myoma

Effect of cabergoline on myoma size and uterine bleeding in women with myomas attending to Arash Hospital

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170917036227N4
Enrollment
50
Registered
2019-06-02
Start date
2019-04-02
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

leiomyoma. Leiomyoma of uterus

Interventions

Intervention 1: Intervention group: 0.5 mg cabergoline tablet (weekly orally, 0.5mg Dostinex tablets per week made in Italy with a generic code of 00562 for 3 months). Intervention 2: Control group: P

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Uterin bleeding and pelvic pain The size of the leiomyoma is between 3 and 8 cm Aged between 20-50 years

Exclusion criteria

Exclusion criteria: Post menopause Pedunculated myoma Use of Hormonal or lipid-lowering agents during the last 6 months History of cardiovascular disease, venous thromboembolism, diabetes mellitus, liver and kidney disorders, hypertension Other malignancies Need or desire for lyomioma surgery in the next 3 months Pregnancy and lactation Uncontrolled hypertension

Design outcomes

Primary

MeasureTime frame
The size of leiomyoma. Timepoint: Before and 3 month after intervention. Method of measurement: Ulthrasonography.;Uterine bleeding. Timepoint: Before and 3 month after intervention. Method of measurement: The number of bleeding days as well as the number of pads used.;Side effects of medication. Timepoint: Before and 3 month after intervention. Method of measurement: check list.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Marzieh Vahid Dastjerdi

Tehran University of Medical Sciences

mvahid@sina.tums.ac.ir+98 21 7771 9922

Outcome results

None listed

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