Standardization of Ayurvedic protocols said during postnatal period in patients.

Randomised control trial(RCT) of sutika paricharya to validate the standard procedures of sutika paricharya - nil

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/07/091300

Enrollment

180

Registered

2025-07-21

Start date

Unknown

Completion date

Unknown

Last updated

2025-08-18

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

Conditions

Health Condition 1: O90- Complications of the puerperium, not elsewhere classified

Interventions

Intervention1: Nil: Nil

Eligibility

Inclusion criteria

Inclusion criteria: Who has uneventful vaginal delivery who screens negative for viral infections like hiv vdrl hbsag

Exclusion criteria

Exclusion criteria: Woman who has delivered abdominally. Who has eventful delivery eclampsia, pre eclampsia, gestational diabetes. Women with chronic diseases like thyroid dysfunction, asthma, epilepsy, cvs, renal or biliary diseases. Woman with compromised mental health. Women with congenital chromosomal or skeletal defects. Who is severely anaemic. Who is under medication foe any mental illness. Women with already existing genital prolapse.

Design outcomes

Primary

Measure	Time frame
To standardize the post natal procedures mentioned in our brihatrayis to standardize the duration of the procedure to standardize the oils, medicines and dietetics to be followed during sutika paricharya.Timepoint: 45 days	—

Secondary

Measure	Time frame
NilTimepoint: Nil	—

Countries

India

Contacts

Public ContactDr Rohit Gokarn

Swaminarayan Ayurveda College

ssackalol@gmail.com9449231730

Outcome results

None listed

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