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A SINGLE ARM CLINICAL TRIAL TO EVALUATE THE EFFICACY OF CHARAKOKTA SUTIKA PARICHARYA A PROOF OF CONCEPT STUDY

A SINGLE ARM CLINICAL TRIAL TO EVALUATE THE EFFICACY OF CHARAKOKTA SUTIKA PARICHARYA A PROOF OF CONCEPT STUDY - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087974
Enrollment
50
Registered
2025-05-30
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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 Health Condition 2: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

None listed

Sponsors

National institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Woman who has undergone full term normal vaginal delivery of age 25-40 years will be selected on Day 1 of postpartum Primipara/Multipara with non complicated full term vaginal delivery

Exclusion criteria

Exclusion criteria: Woman who delivered by cacsarean section or foreeps delivery / vacuum application Antenatal events such as Pregnancy induced hypertension Gestational Diabetes mellitus antepartum haemorrhage eclampsia and pre eclampsia Puerperium associated with complications like severe postpartum haemorrhage retention of placenta Uterine rupture acute inversion of uterus puerperal eclampsia psychosis Septicaemia Preterm delivery or delivery of dead foetus or still born baby Participants with known case of post partum depression Sexually Transmitted diseases Autoimmune disorders haemoglobin less than 7 gm/dl 3rd degree pernieal tear

Design outcomes

Primary

MeasureTime frame
Achievement of pre-pregnant state and overall well being of SutikaTimepoint: 30 days

Secondary

MeasureTime frame
Changes in maternal post partum quality of life.Timepoint: 30 days

Countries

India

Contacts

Public ContactDr Durga pawar

National institute of Ayurveda

durgapawar853@gmail.com09981184965

Outcome results

None listed

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