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Effect of regimen mentioned in Ashtang Sanghraha followed by women after delivery for normal state after delivery.

RANDOMIZED OPEN CONTROLLED CLINICAL STUDY TO EVALUATE THE ADD ON EFFECT OF ASTANG SANGHRAHOKTA SUTIKA PARICHARYA IN THE MANAGEMENT OF SUTIKA W.S.R. TO NORMAL PUERPERIUM. - NIl

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/082354
Enrollment
100
Registered
2025-03-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

None listed

Sponsors

Komal Prakash Patil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Puerperal women irrespective of caste, parity, income group, and occupation will be selected. 2.vaginal delivery cases will be selected.

Exclusion criteria

Exclusion criteria: 1. Women with history of convulsions. 2. Women having severe skin diseases. 3. Women underwent cesarean section

Design outcomes

Primary

MeasureTime frame
To evaluate the add on effect of ashtang sangrahokta sutika paricharya in the management of sutika W.S.R. to normal puerperiumTimepoint: 7 days

Secondary

MeasureTime frame
1) To study the role of ashtang sangrahokta sutika paricharya. 2) To Support health status of mother during puerperal period. 3) To promote Involution of uterus effectively followed by garbhashay shodhana and vatashamana. 4) To study in detail of sutika awastha and the changes which occures during this period by both ayurvedic and modern view. 5) To achieve good lactation and ensure overall well being. 6) To achieve the outcome in 45 days. 7) To assess the changes with body weight, length of uterus from symphysis pubis.Timepoint: 45 days

Countries

India

Contacts

Public ContactDr.Komal Prakash Patil

Yashwant ayurvedic college postgraduate training and Research centre Kodoli

vishalaturlapati@gmail.com9960217429

Outcome results

None listed

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