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Treatment of premature menopause

Comparison of platelet-rich plasma (PRP) injection effects and consumption of Ova Boost on improving ovary function in women with premature ovarian failure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250512065703N1
Enrollment
20
Registered
2025-07-15
Start date
2025-07-23
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Premature menopause. Primary ovarian failure

Interventions

Women diagnosed with premature menopause by a specialist physician, aged between 28 and 35 years, will be enrolled in this study after completing the informed consent form. These participants will und

Sponsors

Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
28 Years to 35 Years

Inclusion criteria

Inclusion criteria: Age range 28-35 Confirmation of premature menopause by a specialist doctor Absence of uterine and ovarian problems Absence of hormonal, cancer and autoimmune diseases Not taking antidepressants and anti-stress medications

Exclusion criteria

Exclusion criteria: Presence of uncontrolled chronic diseases such as heart or kidney failure. Recent history of pelvic or uterine surgery. Severe psychiatric disorders interfering with study participation. Use of medications affecting the hypothalamic-pituitary-ovarian axis. Lack of willingness or inability to complete study follow-up. Any medical condition deemed unsuitable for participation by the investigator.

Design outcomes

Primary

MeasureTime frame
Follicle Stimulating Hormone (FSH) measurement. Timepoint: Before and after the intervention. Method of measurement: VIDAS system.;Estradiol measurement. Timepoint: Before and after the intervention. Method of measurement: VIDAS system.;Anti-Müllerian Hormone ( AMH) measurement. Timepoint: Before and after the intervention. Method of measurement: VIDAS system.;Antral Follicle Count ( AFC). Timepoint: Before and after the intervention. Method of measurement: Ultrasound.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAtena Mansouri

Birjand University of Medical Sciences

mansouri-atena@yahoo.com+98 56 3239 5000

Outcome results

None listed

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