Study the effects of probiotic supplementation on polycystic ovary syndrome

Study the effects of probiotic supplementation on metabolic parameters and level of androgens in women with polycystic ovary syndrome: a randomized double-blind, clinical trial

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180404039187N3

Enrollment

Registered

2019-04-09

Start date

2018-08-23

Completion date

Unknown

Last updated

2019-04-23

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

Conditions

Polycystic ovary syndome. Polycystic ovarian syndrome

Interventions

Intervention 1: Intervention group:daily administration of 1 probiotic capsule "DAILYEAST" for 3 months(a product of zist takhmir company). Intervention 2: Control group:daily administration of 1 pla

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: patients whom have polycystic ovary syndrome based on the ultrasond tests

Exclusion criteria

Exclusion criteria: hypertension Hyperprolactinemia Renal failure Liver failure Heart failure Cancer Diabetes Hyperthyroidism Hypothyroidism Smoking

Design outcomes

Primary

Measure	Time frame
Fasting blood sugar level. Timepoint: At the beginning and 3 months later. Method of measurement: laboratory tests(enzymatic).;Testestrone. Timepoint: At the beginning and 3 months later. Method of measurement: laboratory tests(immuno assay).;Dehydroepiandrosterone sulfate. Timepoint: At the beginning and 3 months later. Method of measurement: laboratory tests(immuno assay).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElnaz Shaseb

Tabriz University of Medical Sciences

elnaz_shaseb_64@yahoo.com+98 144933344198

Outcome results

None listed

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