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Evaluation of the effects of letrozole and cabergoline and GnRH agonist on the size and symptoms of uterine leiomyomas

Evaluation of the effects of letrozole and cabergoline and GnRH agonist on the size and symptoms of uterine leiomyomas

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241122063802N2
Enrollment
90
Registered
2025-09-22
Start date
2025-09-23
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Condition 1: uterine fibromas or leiomyomas. Condition 2: Abnormal uterine bleeding. Leiomyoma of uterus Abnormal uterine and vaginal bleeding, unspecified

Interventions

Intervention 1: Intervention group: Group one will receive letrozole at a dose of 2.5 mg daily for three months. Intervention 2: Intervention group: Group two will receive cabergoline at a dose of 2.5

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 55 Years

Inclusion criteria

Inclusion criteria: Women aged 25 to menopause, defined as 1 year of consecutive absence of menstrual bleeding Uterine fibroids classified as FIGO types 2, 3, 4, and 5 with sizes ranging from 5 to 10 centimeters

Exclusion criteria

Exclusion criteria: Women in menopause, defined as 1 year of consecutive absence of menstrual bleeding, with symptoms of hypoestrogenism having uterine masses with diagnoses other than uterine leiomyoma or suspicion of sarcoma

Design outcomes

Primary

MeasureTime frame
Dimensions and number of leiomyomas. Timepoint: Beginning and end of treatment. Method of measurement: Abdominal or vaginal ultrasound.;Clinical symptoms. Timepoint: Beginning and end of treatment. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Side effects of treatment. Timepoint: Beginning and end of treatment. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Sattarpour

Tabriz University of Medical Sciences

rezasattarpour.tums@gmail.com+98 41 3553 9161

Outcome results

None listed

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