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The effect of clonidine tablets on pregnancy rate in women with polycystic ovary syndrome

Prescribing clonidine tablets as a premedication in patients with polycystic ovary syndrome before entering IVF stages: Evaluation of follicle growth and pregnancy rate

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20111024007883N7
Enrollment
100
Registered
2025-10-29
Start date
2025-11-06
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Polycystic ovary syndrome. Polycystic ovarian syndrome

Interventions

Intervention 1: The intervention group with clonidine tablets: In this intervention study, 100 women with polycystic ovary syndrome will take 0.2 mg of clonidine (a hypertension drug) daily for two mo

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Age 20 to 40 years (of reproductive age) Diagnosis of polycystic ovary syndrome based on the Rotterdam criteria Diagnosis of infertility (at least one year of unsuccessful attempts without using contraception) Having primary infertility The husband have not male infertility

Exclusion criteria

Exclusion criteria: There should be no female reproductive problems of the uterine system, fallopian tubes, etc., as diagnosed by a gynecologist Not having endocrine problems such as thyroid Absence of hormonal disorders (especially in the hypothalamic-pituitary-adrenal axis) Absence of chronic diseases such as illness, kidney failure, disorders of the digestive system organs, etc., as confirmed by a clinician Not taking medications such as injectable insulin No smoking, alcohol, drugs, psychotropic medications Not taking antidepressants Not being obese (BMI less than 27)

Design outcomes

Primary

MeasureTime frame
Pregnancy rate. Timepoint: 2 to 5 pregnancy tests. Method of measurement: Baby check and, if pregnancy is suspected, a blood test to measure beta.

Secondary

MeasureTime frame
Anxiety. Timepoint: Before and after the questionnaire. Method of measurement: Spielberger State-Trait Anxiety questionnaire & Beck anxiety questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarideh Zafari Zangeneh

Tehran University of Medical Sciences

zangeneh14@gmail.com+98 21 6658 1616

Outcome results

None listed

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