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Comparison of the effect of myo-inositol alone and in combination with standard treatment on fertility outcomes in women with polycystic ovary syndrome undergoing IVF treatment

Comparison effect of myoinositol supplement alone and with metformin and sitagliptin in infertile women with polycystic ovary syndrome treated with IVF

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240303061157N2
Enrollment
125
Registered
2025-10-09
Start date
2025-10-23
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

Polycystic ovary syndrome. Polycystic ovary syndrome

Interventions

Intervention 1: Control group: They will receive 500 mg of metformin daily. Intervention 2: First intervention group: They will receive 2 grams of myo-inositol daily. Intervention 3: Second interventi

Sponsors

Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Infertile women with classic polycystic ovary syndrome

Exclusion criteria

Exclusion criteria: Patients with hypersensitivity to metformin Patients with hypersensitivity to dipeptidyl peptidase-4 inhibitors Male-related infertility Patients with congenital adrenal hyperplasia Patients with thyroid gland disorders Patients with Cushing's syndrome Patients with androgen-secreting neoplasia Patients with severe liver disease Patients with severe kidney disease Patients with gallstones

Design outcomes

Primary

MeasureTime frame
No. of Oocyte retrieved. Timepoint: Once, in day of puncture. Method of measurement: Oocyte retrieval will be performed by ultrasound-guided transvaginal aspiration using a single-lumen needle.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactForogh Forghani

Zahedan University of Medical Sciences

f.forghani@zaums.ac.ir+98 54 3337 2013

Outcome results

None listed

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