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Compare two interventional group to study the efficacy of Pippali churna and Vidarikand Churna in the management of stanyakshay

Radomised comparative clinical study to evaluate the efficacy of Pippali Churna and Vidarikand Churna in the management of Stanyakshay - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/085341
Enrollment
80
Registered
2025-04-22
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: O924- Hypogalactia

Interventions

None listed

Sponsors

Dr Sheela Natharo Bhalerao
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of Stanyakshaya in Sutika Awastha. 2. Age group of patients between 19-35 years. 3. Patients after delivery up to 3 months 4. Sutika with breast feeding frequency less than 6-7 times a day. 5. Patient having history of lactational deficiency

Exclusion criteria

Exclusion criteria: Known patients of systemic disorder like renal failures , hepatic disorder Antomical pathologies of mother like engorgement,cracked nipples, mastitis, flat/inverted nipples Mothers having stanya dushti, Baby having infectious diseases, Infant with cleft palate, Infant with disorganized sucking reflex

Design outcomes

Primary

MeasureTime frame
There is no significant difference between Pippali churna and Vidarikand churna in the management of stanyakshayTimepoint: 0,7th,14th,21th days

Secondary

MeasureTime frame
Vidarikand churna is better than Pippali churna in the management of stanyakshayTimepoint: 0,7th,14th,21th days;Pippali Churna is better than Vidarikand churna in the management of stanyakshayTimepoint: 0,7th, 14th, 21th days

Countries

India

Contacts

Public ContactDr Prasad Lomte

Late Kedari Redekar Ayurvedic Mahavidyalay Gadhinglaj Kolhapur Prasuti evum Striroga department

prasad.lomate969@gmail.com8275917687

Outcome results

None listed

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