A clinical study to evaluate the efficacy of vranaropankar churna in the treatment of suddha vrana

Randomized controlled clinical trial to evaluate the ropan effect of vranaropankar churna local application in the management of shuddha vrana - nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/11/077292

Enrollment

Registered

2024-11-25

Start date

Unknown

Completion date

Unknown

Last updated

2024-12-09

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

Conditions

Health Condition 1: L989- Disorder of the skin and subcutaneous tissue, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients having vrana in shudha awastha.2) Patients having wound with depth less than 1cm.3) Patients irrespective of sex, religion, occupation etc4) Dimension of wound up to 30sq.cm.5)Patients either Age between 18 to 60 years.6)Patients having wounds on extremities only

Exclusion criteria

Exclusion criteria: 1)Wounds which are dushta.2)Patients having bleeding disorder3) Wounds of size more than 30sq.cm.4) known case of AIDS, DM, Hepatitis B., TB and immunocompromised people5) Patient having wound with depth more than 1cm.

Design outcomes

Primary

Measure	Time frame
To study the efficacy of Vranaropankar Churna in the treatment of shuddha vrana after 15daysTimepoint: 15 days study with alternate day dressing and follow up and wound assessment will be done on 0th,5th,10th and 15th day.	—

Secondary

Measure	Time frame
To study the ropan effect of vranaropankar churna after 15 days of of interventionTimepoint: 15 days study with alternate day dressing & wound assessment will be done on 0th,5th,10th & 15th day	—

Countries

India

Contacts

Public ContactUmesh Abhiman Paikrao

MES Ayurveda Mahavidyalaya

dr.ashok2575@yahoo.com9422032696

Outcome results