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Treatment of uterine myoma.

Evaluation of the effect of cabergoline (dopamine receptor agonist) on the size and symptoms of uterine myoma in women with myoma.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201403092624N12
Enrollment
50
Registered
2014-04-12
Start date
2014-03-11
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

fibromyoma of uterus. Leiomyoma of uterus

Interventions

Intervention 1: Intervention group:prescription of weekly 0.5 mg cabergoline for 3 months. Intervention 2: Control group: monitoring without drug prescription for 3 months.
Treatment - Drugs
Intervention group:prescription of weekly 0.5 mg cabergoline for 3 months.
Control group: monitoring without drug prescription for 3 months.

Sponsors

Vice chancellor for research ,Iran University of Medical Sciences.
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: symptomatic myoma including abnormal uterine bleeding ( after excluding the other etiologies), pelvic pain, and myoma in ultrasound with a minimum size of 2 centimeters. Exclusion criteria : severe bleeding; pregnancy; breast feeding; using any hormone or sedative; any other pathology in ultrasound; any known hormonal problems and any conditions need to an emergency treatment.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Change in the size of myoma. Timepoint: 3 months after treatment. Method of measurement: Ultrasound.

Secondary

MeasureTime frame
Change of the symptoms including pelvic pain and amount of bleeding. Timepoint: 3 months after treatment. Method of measurement: Questionair and VAS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Kashanian

Iran University of Medical Sciences

maryamkashanian@yahoo.com+98 21 5563 3244

Outcome results

None listed

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