To Study The Efficacy Of Ashwagandha Ghrita and PRP in improving Depressed Scars.

A Randomized Comparative Clinical Study In The Age Group Of 18 to 45 years To Assess The Efficacy Of Ashwagandha Ghrita With Vedhan Karma and PRP With Vedhan Karma In The Management of Atrophic Scars w.s.r. to Utsadan Karma. - NIL

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/01/101896

Enrollment

Registered

2026-01-23

Start date

Unknown

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

Health Condition 1: L909- Atrophic disorder of skin, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with clinically diagnosed atrophic scars (post acne, traumatic scars, post operative scars). 2. Scar grades between mild to severe atrophic scars (based on Goodman and Boron Classification). 3. Willing to undergo treatment and follow up. 4. Patients who give written informed consent to participate in study.

Exclusion criteria

Exclusion criteria: 1. Active skin infections like acne or dermatitis in treatment area. 2. History of keloid formation or hypertrophic scars. 3. Bleeding disorders or patients on anticoagulant therapy. 4. Patients with systemic illness like uncontrolled diabetes, HIV, hepatitis. 5. Pregnant or lactating woman. 6. Patients on isotretinoin therapywithin the last 6 months. 7. Atrophic Scars on muscles, bone and cartilages.

Design outcomes

Primary

Measure	Time frame
The parameters will be noted down before and after treatment. 1. Scar surface appearance 2. Height 3. Colour mismatchTimepoint: Total duration of study 30 days. 1st, 15th and 30th day. final follow up on 45th day.	—

Secondary

Measure	Time frame
1. No Improvement- 0% relief 2. Poor Improvement- 0% to 25% relief 3. Mild Improvement- 26% to 50% relief 4. Moderated Improvement- 51% to 75% relief 5. Marked Improvement- 76% to 100% reliefTimepoint: 30 Days study 1st,15th and 30th day. final assessment on 45th day.	—

Countries

India

Contacts

Public ContactDr Nikita Balwantrao Kapse

Dayabhai Maoji Majithiya Ayurved Mahavidyalaya, Yavatmal

drviharbidwai@gmail.com9822299174

Outcome results