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Investigating the effect of probiotics on menstrual disorders and anti-mullerin hormone levels in patients with polycystic syndrome type A and B

Investigating the effect of probiotics on menstrual disorders and anti-mullerin hormone levels in patients with polycystic syndrome type A and B

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251127068135N1
Enrollment
100
Registered
2026-05-02
Start date
2026-05-22
Completion date
Unknown
Last updated
2026-06-01

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: 50 people with polycystic ovary syndrome type A and B will be in the intervention group, who will take one FemiCare probiotic daily for 12 weeks,.After 12 weeks, the anti-Mullerian hor

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Confirmed diagnosis of PCOS based on established criteria (such as the Rotterdam criteria) AMH above 3.5

Exclusion criteria

Exclusion criteria: Other important medical conditions that affect hormone levels or gut microbiota Use of medications that affect hormonal levels or gut microbiota

Design outcomes

Primary

MeasureTime frame
Anti mullerian hurmon. Timepoint: 12weeks. Method of measurement: In-vitro quantitative measurement.

Secondary

MeasureTime frame
The sound is muffled. Timepoint: 12weeks. Method of measurement: Clinical examination.;Hormonal pattern hair loss. Timepoint: 12weeks. Method of measurement: Clinical examination.;Acne. Timepoint: 12weeks. Method of measurement: Clinical examination.;Breast reduction. Timepoint: 12weeks. Method of measurement: Clinical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyedeh Zahra Hashemi

Shahid Beheshti University of Medical Sciences

zahra.hash71@gmail.com+98 21 2303 1307

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026