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Post-partum pain after normal vaginal delivery

A comparative study between yavakshar and shunthi churna in sutika makkal shoola - post partum pain

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/07/026493
Enrollment
60
Registered
2020-07-10
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: O908- Other complications of the puerperium, not elsewhere classified Health Condition 2: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

Intervention1: yavakshar: oral administration of yavakshar 250mg BD with goghrit for 5 days then 2 follow ups with medication and 1 without medication. Control Intervention1: Shunthi churna: oral admi

Sponsors

Depatment of Prasuti Tantra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: both primi and multi gravida who have undergone normal vaginal delivery with lower abdominal pain as complaint with no other post-partum complications

Exclusion criteria

Exclusion criteria: patients who have undergone caesarean section, suffering from any chronic illness, any psychological condition, any complication like deep perineal tear, P.P.H., any allergy to drug.

Design outcomes

Primary

MeasureTime frame
Assessment will be done on the basis of prepared proforma and improvement in the sign and symptoms of Makkal shoola.Timepoint: Drug will be given just after vaginal delivery for 5 days, then 2 follow ups at an interval of 7 days with medication and last follow up without medication.

Secondary

MeasureTime frame
Improvement in VAS rating and Numeric pain scale ratingTimepoint: Drug will be given just after vaginal delivery for 5 days, then 2 follow ups at an interval of 7 days with medication and last follow up without medication.

Countries

India

Contacts

Public ContactDr Sunita Suman

Institute of Medical Sciences, Faculty of Ayurveda

ssom18@gmail.com

Outcome results

None listed

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