To check the clinical efficacy of Pinda Taila and its Liniments in case of Gathiya Roga.

A Comparative Pharmaceutical Clinical Study Of Pinda Taila and Its New Dosage Form Pinda Taila Liniment With Special Reference To Vatarakta - Nil

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/12/099534

Enrollment

Registered

2025-12-19

Start date

Unknown

Completion date

Unknown

Last updated

2026-01-12

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

Conditions

Health Condition 1: M109- Gout, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Disease presenting with classical clinical feature of Vatarakta like, Sandhi shool (Joint pain), Sandhi shotha (Swelling of joint), Sparsha asahatvam (Tenderness), Raga (Redness), Twak vaivarnya (Discolouration of skin) and Vidaha(Burning sensation).

Exclusion criteria

Exclusion criteria: 1 Patients below the age of 20 years and above 60 years of age. 2 Patient having chronic symptoms of Vatarakta along with other deformities. 3 Patients who are suffering from any other form of arthritis like Osteoarthritis, Tubercular Arthritis, Rheumatoid Arthritis etc. 4 Patients who are suffering from chronic renal, respiratory, cardiac or hepatic disorder. Patients who haver any malignancy. 5 Patients who are pregnant and lactating mothers.

Design outcomes

Primary

Measure	Time frame
Mild to moderate symptomatic improvement in Pain, swelling and tenderness of diagnosed Vatarakta patient.Timepoint: on 7th days and 14th days	—

Secondary

Measure	Time frame
Relief in Redness,Tenderness Swelling Of Joint,Discolouration of skinTimepoint: 14 days	—

Countries

India

Contacts

Public ContactDr Manish Mishra

Government PG Ayurvedic College And Hospital Varanasi,Uttar Pradesh 221002

drankitg01@gmail.com9532016160

Outcome results