Effect of a transdermal ayurvedic patch for pain and swelling relief in sprain injuries.

A randomized controlled clinical study to evaluate the efficacy of vedanahar transdermal patch in the management of aghataja shoth with special reference to sprain. - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/04/109080

Enrollment

Registered

2026-04-22

Start date

Unknown

Completion date

Unknown

Last updated

2026-04-27

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

Conditions

Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Clinical diagnosis of acute sprain (ankle or wrist or knee). Able to give informed consent and regular followup. Acute pain within 24 hrs of injury. People of all caste, age, religion and sex. Controlled dm type 2 Immunocompromised patients.

Exclusion criteria

Exclusion criteria: Open wounds or skin inection at site of application. Known allergy to patch components in either group. Use of systemic nsaids or steroids within 24-48 hours prior. Chronic pain or known systemic inflammatroy disease, pregnancy, lactation, severe hepatic or liver disease. Grade II and III sprain requiring surgical intervention. Known fractures.

Design outcomes

Primary

Measure	Time frame
analgesic effect of Vedanahar transdermal patchTimepoint: Day 1, Day 2, Day3, Day 5, Day7	—

Secondary

Measure	Time frame
Improvement in range of motion (ROM) of the affected area. Timepoint: Day 1, Day 2, Day3, Day 5, Day7	—

Countries

India

Contacts

Public ContactDr Pradnya Kapse

R A Podar Ayurved Medical College Worli Mumbai

rasrajk@gmail.com9930939867

Outcome results