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The effect of magnesium supplements on polycystic ovarian syndrome (PCOS)

The effect of magnesium supplements on clinical and metabolic variables in women with polycystic ovarian syndrome (PCOS)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200115046147N1
Enrollment
40
Registered
2020-02-01
Start date
2020-01-28
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

polycystic ovarian syndrome (PCOS).

Interventions

Intervention 1: Intervention group: In the magnesium group, magnesium oxide supplement made by Galen's company in the form of 250 mg a day for two months will be given to patients and in the control g

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Patients with polycystic ovary syndrome based on the Rotterdam Diagnostic Criteria2. Satisfaction with attending the study3. Satisfaction to continue cooperation4. Magnesium does not have a high base normal.5. There is no history of electrolyte abnormalities associated with potassium or calcium in the patient.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Changes in Insulin Resistance Index (HOMA-IR). Timepoint: FBS and serum insulin are re-administered to patients at baseline and after 2 months of treatment (end of treatment). Method of measurement: ice.Patients receive fasting insulin for a 12-hour fasting blood sample to measure fasting blood sugar (for diabetes screening).

Secondary

MeasureTime frame
Weight Loss and Blood Glucose and Lipid Profile and Blood Pressure and Menstrual Cycle Adjustment in Magnesium Supplemented Patients. Timepoint: After 2 months of treatment (end of treatment), weight, waist circumference, blood pressure, menstrual pattern and serum levels of FBS, TG, CHOL, LDL, HDL and insulin are monitored again for two months after completion. Patients will be monitored for clinical symptoms including menstruation, weight, waist circumference and blood pressure. Method of measurement: The pattern of menstrual periods is recorded in a questionnaire designed for the duration and duration of bleeding during the menstrual cycle. After fasting for 12 hours, a blood sample was taken to measure fasting blood sugar (for diabetes screening), fasting insulin and Mg levels, as well as TG, CHOL, HDL and LDL. People are included in the study who do not have high normal magnesium levels. Weight in fasting, without shoes, with minimal clothing and measured using the Seca Digital Balance with a accuracy of 0.1 kg. Height is measured with the help of a tape measure with a accuracy of 0.1 cm. BMI is calculated by dividing the weight in kilograms by the power of 2 heights per meter. Waist circumference greater than 5 cm above the navel and hip circumference less than 5 cm below the navel are measured with tape measure. Patients' blood pressure is measured and recorded with a single device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShabnam Shahmoradi

Zanjan University of Medical Sciences

ashkanghadimi23@gmail.com+98 24 3344 0932

Outcome results

None listed

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