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Investigating the effect of magnesium supplementation on stress and ovulation

The Investigating the effect of magnesium supplementation on stress and ovulation rate in infertile women with polycystic ovary syndrome

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20091229002924N3
Enrollment
108
Registered
2024-01-17
Start date
2024-02-20
Completion date
Unknown
Last updated
2024-01-22

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: The intervention group receives magnesium supplements twice a day in the form of magnesium oxide tablets (each tablet contains 250 mg of elemental magnesium). Inter

Sponsors

Bojnourd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Infertility for more than a year Absence of acute and chronic diseases, Not using medicinal compounds and supplements containing magnesium. Not taking anti-anxiety and sedative drugs. Not using drugs, tobacco and alcohol. Not using relaxation techniques. Body mass index less than 35, Magnesium intake less than 75% of the recommended dietary intake

Exclusion criteria

Exclusion criteria: Pregnancy, Use of oral contraceptive pills, Occurrence of any severe stress (for example, divorce or death of a relative), Personal desire to withdraw from the study during the study, Consumption of less than 90 out of 112 magnesium supplement tablets or placebo.

Design outcomes

Primary

MeasureTime frame
To determine the effect of magnesium supplementation on stress and ovulation rate in infertile women with polycystic ovary syndrome. Timepoint: Newton's stress questionnaire first and then 4 weeks after taking the pills and at the end of taking the pills.Vaginal ultrasound at the beginning of the study as an entry criterion and then 4 weeks after taking the pills and then between the 10th and 14th day of the trigger drug cycle. Method of measurement: Ultrasound, Newton stress questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Hassanzadeh Bashtian

Bojnourd University of Medical Sciences

m.h.Bashtian@gmail.com+98 58 3229 7097

Outcome results

None listed

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