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A clinical study to evaluate the effect of Sootika Paricharya explained by Charakacharya in postnatal mothers

Clinical evaluation of the effect of Charakokta Sootika Paricharya - CCSP

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/11/010702
Enrollment
100
Registered
2017-11-29
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- Post-natal patients who have undergone normal vaginal delivery

Interventions

Intervention1: TRIAL GROUP: Ushna jala parisheka, Snehapana with accha ghrita and panchakola churna, Sthanika abhyanga, Udara patta bandhana, Yavagu Pana Control Intervention1: CONTROL GROUP: Normal d

Sponsors

Dr Jyoti Mallappa Kumbar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients fulfilling diagnostic criteria of Sootika Patients with full term normal vaginal delivery Patients with episiotomy wound, perineal tear

Exclusion criteria

Exclusion criteria: Systemic disorders like Diabetes, Tuberculosis etc. Patients with L.S.C.S. Conditions like retention of placenta, PPH, IUD, inversion or prolapse of uterus

Design outcomes

Primary

MeasureTime frame
Involution of uterus Abdominal wall circumference Episiotomy wound healing Timepoint: Involution of uterus Abdominal wall circumference Episiotomy wound healing—

Secondary

MeasureTime frame
Back ache Perineal pain Lactation After pain Lochia discharge Breast engorgement Timepoint: 35 days—

Countries

India

Contacts

Public ContactDr Jyoti Mallappa Kumbar

Parul Institute of Ayurved

drjyotik11@gmail.com9482628541

Outcome results

None listed

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