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To study the effect of probiotics in management of Poly cystic ovarian syndrome

Efficacy of probiotic based dietary and lifestyle regime in management of PCOS cases

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/07/007086
Enrollment
104
Registered
2016-07-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Poly cystic ovary syndrome (PCOS)

Interventions

Intervention1: probiotic group: Probiotics as capsule Diet and lifestyle counselling SIM on nutrition and lifestyle Dose - Each pill will contain 10 billion live organisms. One capsule per day for

Sponsors

ICMR scholarship
Lead Sponsor
ProvinormUnique Biotech Hyderabad
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Diagnosed with PCOS by Rottadom Criteria Aged between 18 to 45 years BMI below 45 Physician approval for selected patient. Able to read Willingness to provide informed consent and to visit hospital for follow up

Exclusion criteria

Exclusion criteria: Any pre existing condition or contraindications for example CAD, abnormal creatinine levels, liver dysfunction Immunosuppressant cases Bedridden patients and patients due for operations Enrolled in other active intervention research studies Post menopausal women Women with hysterectomy Smoking or drug addicts or with psychiatric illness

Design outcomes

Primary

MeasureTime frame
1. Anthropometric factors Weight BMI Adiposity distribution (by measures including waist circumference, waist-to-hip ratio (WHR)) 2. Reproductive factors Menstrual regularity (an initiation of menses or significant shortening of cycle length where possible) Clinical hyperandrogenism (hirsutism assessed clinically by Ferriman-Gallwey score (FG) 3. LPS levels 4. Metabolic factor â?? Fasting glucose, Fasting insulin, Testosterone 5. Quality of life and participant satisfaction Timepoint: baseline / pre-intervention and post intervention

Secondary

MeasureTime frame
Quality of life and participant satisfaction Timepoint: Pre and post intervention

Countries

India

Contacts

Public ContactIshwarpreet kaur

PGIMER, Chandigarh

ishwarpreet814@yahoo.co.in9888504895

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 14, 2026