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The effect of Vitagnos tablets on the function of polycystic ovaries

The effect of Vitagnus tablets on follicle number and size, endometrial thickness and fertility in infertile women with polycystic ovary syndrome

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200831048569N1
Enrollment
60
Registered
2020-10-29
Start date
2020-11-21
Completion date
Unknown
Last updated
2020-11-30

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: Intervention group: Control group: From the beginning of the monthly cycle, they take 1 mg of folic acid tablets and one empty capsule (placebo) daily. The use of this pill and placebo

Sponsors

Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Age 18 to 35 years Having written consent to participate in the study Infertility is known to cause polycystic ovary syndrome and rule out other causes of infertility Ultrasound-confirmed polycystic ovaries along with another Rotterdam criteria No other androgenic disorders such as adrenal hyperplasia or androgen-producing tumor Manifestations of hyperandrogenism (high testosterone) No diseases such as: hypothyroidism or hyperthyroidism, hyperprolactinemia, kidney, heart, liver, bone diseases, pituitary tumor, cancer and diabetes Do not take infertility drugs or any other hormonal drugs in the last three months Body mass index 18 to 35 Hypersensitivity to food and drugs such as lactose, letrozole and vitagnus

Exclusion criteria

Exclusion criteria: Breastfeeding Smoking and drugse Stressful events in the last three months Previous surgery on one or both ovaries Taking haloperidol

Design outcomes

Primary

MeasureTime frame
Number of follicles. Timepoint: Before the intervention and 1/5 month after the intervention. Method of measurement: Sonography.;Follicle size. Timepoint: Before the intervention and 1/5 month after the intervention. Method of measurement: Sonography.;Endometrial thickness. Timepoint: Before the intervention and 1/5 month after the intervention. Method of measurement: Sonography.;Fertility rate. Timepoint: Before intervention and 2 months after intervention. Method of measurement: BHCG test.

Secondary

MeasureTime frame
Improve ovarian function. Timepoint: After the intervention. Method of measurement: sonography.;Side effects. Timepoint: During and after the intervention. Method of measurement: check list.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVahideh Behmard

Gonabad University of Medical Sciences

vahideh.behmard@gmail.com+98 71 3731 7895

Outcome results

None listed

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