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Assesment the clinical effect of myoinositol on insulin resistence in women with PCOS

Assesment the clinical effect of myoinositol on insulin resistence in women with PCOS

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015010319426N4
Enrollment
50
Registered
2015-01-17
Start date
2015-01-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Polycystic Ovarian Syndrome. Ovarian dysfunction, unspecified

Interventions

Patients with dignosis of PCOD under treatment with myoinositol (powder) 4 gram daily for three months and primary and secondary outcome measure before and after reatment.
Treatment - Drugs
Patients with dignosis of PCOD under treatment with myoinositol (powder) 4 gram daily for three months and primary and secondary outcome measure before and after reatment

Sponsors

Vice chancellor for research, Shahid Beheshti University of Medical Science
Lead Sponsor
Healthparsian. com
Collaborator

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: women who were between 20 and 40 years old, and had PCOS diagnosed by a gynecologist. Exclusion criteria: patients who were diagnosed with Cushing syndrome, congenital adrenal hyperplasia, hyperprolactinemia, hypothyroidism, hyperthyroidism, androgen secreting tumor; medications known to affect metabolic parameters, such as metformin and corticosteroids.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Fasting glucose. Timepoint: Before intervention and three months after treatment. Method of measurement: Blood serum.;Fasting insulin. Timepoint: Before intervention and three months after treatment. Method of measurement: Blood serum.;HOMA IR. Timepoint: Before intervention and three months after treatment. Method of measurement: Calculation by formola.

Secondary

MeasureTime frame
Weight. Timepoint: Before intervention and three months after treatment. Method of measurement: Balance.;Height. Timepoint: Before intervention and three months after treatment. Method of measurement: Meter.;Body Mass Index. Timepoint: Before intervention and three months after treatment. Method of measurement: Formola.;Low density lipoprotein. Timepoint: Before intervention and three months after treatment. Method of measurement: Blood serum.;High density lipoprotein. Timepoint: Before intervention and two months after vitamin D injection. Method of measurement: Blood serum.;Free testosterone. Timepoint: Before intervention and two months after vitamin D injection. Method of measurement: Blood serum.;Dehydoepiandrasteione. Timepoint: Before intervention and two months after vitamin D injection. Method of measurement: Blood serum.;Triglyceride. Timepoint: Before intervention and two months after vitamin D injection. Method of measurement: Blood serum.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Saghar salehpour

Infertility & Reproductive Health Research Centre - Shahid Beheshti of Medical Science

saghar.salehpour2014@gmail.com+98 21 2243 2558

Outcome results

None listed

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