Ayurveda oil application for healing of the wound due to minor procedure during normal delivery

Randomised controlled trial to evaluate the wound healing potential of Dineshavallyadi Taila on episiotomy wound - Nil

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/05/110740

Enrollment

Registered

2026-05-20

Start date

Unknown

Completion date

Unknown

Last updated

2026-06-01

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

Conditions

Health Condition 1: O80- Encounter for full-term uncomplicated delivery

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects underwent episiotomy regardless of parity. 2. Subjects with cephalic presentation in whom episiotomy was performed, including both term and preterm births. 3. Subjects with single pregnancy. 4. Subjects willing to give written consent

Exclusion criteria

Exclusion criteria: 1. Subjects with 3rd and 4th degree perineal tear. 2. Subjects who are hypersensitive to any of the drugs of Dineshavalyadi Taila. 3. Subjects who are contraindicated for the NSAID included in the study protocol.

Design outcomes

Primary

Measure	Time frame
Improvement in perineal pain assessed through VAS scale and pain catastrophising scale compared to control group. Improvement in wound healing in terms of discharge, oedema and approximation compared to control group. Timepoint: Day 0 and Day 14	—

Secondary

Measure	Time frame
Requirement of analgesic medication compared to control groupTimepoint: Day 0, 2, 7 and 14; Change in EQ-5D-5L questionnaire score compared to control groupTimepoint: Day 0, 7 and Day 14	—

Countries

India

Contacts

Public ContactDr Vrinda

Rashtrotthana Research Centre,

vrindabhat89@gmail.com09035996258

Outcome results