Preparation of a medicated plaster using medicated oil "Murivenna Taila" and its use in the condition of sprains.

Exploratory study on modification of Murivenna taila to a medicated plaster

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/04/013225

Enrollment

Registered

2018-04-12

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: null- Sprain

Interventions

Intervention1: Murivenna Medicated PLaster: 1.Application for 7 days 2.Fresh plaster each day 3.External application on the site of sprain Control Intervention1: Murivenna taila application Dose- dep

Eligibility

Inclusion criteria

Inclusion criteria: Patients with acute sprain

Exclusion criteria

Exclusion criteria: 1.Patients with fracture or dislocation of joints 2.Patients with previous history of ligament or bony reconstructive surgery 3.Patients with other orthopedic injuries at the time of presentation 4.Patients with gross swelling 5.Patients with diminished sensation in legs 6.Patients with other systemic diseases

Design outcomes

Primary

Measure	Time frame
1.Pain 2.Discolouration 3.Swelling Timepoint: 8th day	—

Secondary

Measure	Time frame
1. Pain scale grading 2. Range of movement of jointTimepoint: 8th day	—

Countries

India

Contacts

Public ContactDr Vinay Kadibagil

Sri Dharmasthala Manjunatheshwara College of Ayurveda and Hospital

drvinaykadibagil@gmail.com9986596107

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026