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A COMPARATIVE STUDY TO EVALUATE THE EFFECT OF DIFFERENT MODES OF SHODHANA FOLLOWED BY SHIVA GUTIKA IN POLYCYSTIC OVARIAN SYNDROME

A COMPARATIVE CLINICAL STUDY TO EVALUATE THE EFFECT OF VAMANA AND VIRECHANA FOLLOWED BY SHIVA GUTIKA IN POLYCYSTIC OVARIAN SYNDROME - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093403
Enrollment
200
Registered
2025-08-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: E889- Metabolic disorder, unspecified

Interventions

None listed

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion Criteria Female patients in between 16 to 45 years of age Patiems with signs and symptoms of PCOS as enumerated in modified Rotterdam criteria in which PCOS diagnosed if any two of the following are present Clinical or biochemical hyperandrogenism Evidence of oligo-anovulation and oligoamenorrhoea Polycystic appearing ovarian morphology on ultrasound Subjects fit for Snehapana Vamana and virechana based on the group selected

Exclusion criteria

Exclusion criteria: Patient below 16 and above 45 years of age Patients with thyroid dysfunction Patients with Hyperprolactenaemia Patients with congenital anomalies of reproductive system Patients having any other systemic illness like tuberculosis carcinoma Patient having any major renal or liver disorders

Design outcomes

Primary

MeasureTime frame
Regularization of the Menstruation and improving the quantity of Menstrual flow Timepoint: After 60 days of intervention

Secondary

MeasureTime frame
Reduction in the ovarian volume on the repeat abdomen and pelvic scanTimepoint: After 60 days of intervention

Countries

India

Contacts

Public ContactDr Papiya Jana

Sri Kalabyraveshwara Swamy Ayurvedic Medical College Hospital and Research Centre

drpapiya@gmail.com9886716216

Outcome results

None listed

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