To study effect of noola taila as ropan in Agantuj Vrana i.e,Fresh wound

A OPEN RANDOMISED CLINICAL CONTROL TRIAL OF NOOLA TAILA AS ROPAN EFFECT IN AGANTUJ VRANA.

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/12/038497

Enrollment

Registered

2021-12-08

Start date

Unknown

Completion date

Unknown

Last updated

2022-02-21

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

Conditions

Health Condition 1: S809- Unspecified superficial injury ofknee and lower leg

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of both gender in age group18- 70 years included. 2. Irrespective of sex,religion, geographic and economic status. 3. Patients of fresh wound included. 4. Wound size within length 5 cm and breath 5 cm. 5. Depth is not more than 1cm.

Exclusion criteria

Exclusion criteria: a) The age group below 18 years and above 70 years. b) Tubecular ulcer. c) Diabetic ulcer. d) Wound with cyst. e) DVT f) Tubecular ulcer. g) Ulcer due to radition therapy. h) Previously suture wound if infected.

Design outcomes

Primary

Measure	Time frame
Noola Tail is effective as ropan in Agantuj vranaTimepoint: 15 days	—

Secondary

Measure	Time frame
kampillak Sidha Til tila as ropan effective in Agantuj VranaTimepoint: For 15 days ,follow up -alternate day	—

Countries

India

Contacts

Public ContactMadhuri Vijay Jagtap

Hon Shri Annasaheb Dange Ayurved Medical college And post Graduate and Reaserch center ,Ashta

dr.patilmanoj77@gmail.com9422613195

Outcome results