A clinical study to compare the effect of Jatukarnokta Sahachar Taila and Charkokta Sahachar Taila Matra Basti in the management of knee osteoarthritis.

A randomised controlled clinical trial to evaluate the efficacy of Jatukarnokta Sahachar Taila and Charkokta Sahachar Taila Matra Basti in the management of Janu Sandhigata Vata. - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/03/106600

Enrollment

Registered

2026-03-19

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-30

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

Conditions

Health Condition 1: M179- Osteoarthritis of knee, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients showing classical symptoms of Janu Sandhigata Vata for duration of more than 6 months. 2.Janu Sandhi Shool (Knee joint pain). 3.Janu Sandhi Shotha (swelling). 4.Akunchan- Prasaran Vedana (pain during flexion and extension) 5.Vatapurna Druti Sparsha (crepitus) 6.Gender- Male and Female. 7.Age-30 years-70 years. 8.Patient Arha for Basti karma.

Exclusion criteria

Exclusion criteria: 1.Congenital deformities involving Janu Sandhi. 2.Fracture of knee joint needing surgical correction. 3.Auto immune diseases like SLE etc. 4.Neoplasms 5.Permanent joint damage. 6.K/C/O HIV, PTB, Extra-PTB involving knee joint or any other majopr illness 7.K/C/O cardiac or neurological disorders 8.Having severe crippling deformity. 9.Pregnant or lactating women. 10.Contraindications for Snehan or Basti karma in the respective group

Design outcomes

Primary

Measure	Time frame
To clinically evaluate and compare the efficacy of Jatukarnokta Sahachar Taila Matra Basti and Charkokta Sahachar Taila Matra Basti in the management of Janu Sandhigata VataTimepoint: Duration of study 36 months Duration of treatment 7 days Follow up on 7th 21st 49th and 90th day	—

Secondary

Measure	Time frame
To observe adverse effects if anyTimepoint: Duration of study 36 months Duration of treatment 7 days Follow up on 7th 21st 49th and 90th day	—

Countries

India

Contacts

Public ContactDr Aditi Ashok Lingayat

RSMs Centre for postgraduate studies and research in Ayurved, Tilak Ayurved Mahavidyalaya, Pune

ayurvedapune@gmail.com9823050402

Outcome results