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Evaluation of Cabergoline Effectiveness on Fertility of Patients with Adenomyosis

Evaluation of Cabergoline Effectiveness on Infertile Patients with Adenomyosis Undergoing Freeze Embryo Transfer

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20260209068816N1
Enrollment
60
Registered
2026-05-05
Start date
2026-04-21
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Condition 1: Infertility. Condition 2: Adenomyosis. Female infertility Adenomyosis of the uterus

Interventions

Intervention group: Cabergoline 0.5mg twice weekly for 3 months + GnRH agonist protocol.

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 42 Years

Inclusion criteria

Inclusion criteria: Trying to conceive for more than 6 months without success Age: 30-42 years. Diagnosis of adenomyosis on ultrasound. Regular menstrual cycles of 24-35 days. Body Mass Index (BMI) between 19 and 30 (19 < BMI < 30). Having two Grade A oocytes by age 40 and three Grade A oocytes between the ages of 41-42.

Exclusion criteria

Exclusion criteria: Use of infertility treatments in the last 6 months. Previous history of 2 failed embryo transfers. Pelvic pathologies other than uterine adenomyosis. Previous history of hypersensitivity to cabergoline.Intolerance to cabergoline side effects during the study. Failure of ovulation induction and transfer to the uterus during the study. Severe spermatogenesis disorder (azoospermia) in the patient's partner.

Design outcomes

Primary

MeasureTime frame
Implantation Rate. Timepoint: 1 week after positive test of Bhcg. Method of measurement: Sonography.;Biochemical Rate. Timepoint: Two weeks after embryo transfer. Method of measurement: Serum Level of Bhcg.;Clinical Pregnancy Rate. Timepoint: 2 weeks after positive test of Bhcg. Method of measurement: Sonography.;Miscarriage Rate. Timepoint: Early 20 weeks of pregnancy. Method of measurement: Taking patient medical history and Sonography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLida Shafieyan

Tehran University of Medical Sciences

shafieyan.lida@gmail.com+98 21 7788 3285

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026