Comparative Study to Evaluate the Effect of Janubasti Therapy with Til Tail and Haridradi Tail along with Abhadi Churna in Patients of Knee Osteoarthritis

A Comparative Clinical Study To Evaluate The Efficacy Of Janubasti With Tila Taila And Haridradi Taila Along With Abhadi Churna In Cases Of Janugata Sandhivata With Special Reference To Knee Osteoarthritis - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/04/109209

Enrollment

Registered

2026-04-23

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: M179- Osteoarthritis of knee, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex (male/female). Age group 40 70 years. Patients having classical signs & symptoms of Janugata Sandhivata such as: Knee joint pain (Janu Sandhi Shoola) Stiffness (Sandhi Stabdhata) Crepitus Restricted movement Patients diagnosed with Knee Osteoarthritis based on: Clinical findings Radiological evidence (X-ray showing osteophytes, reduced joint space, etc.) Patients willing to participate and give written informed consent. Patients ready to follow trial protocol and attend regular follow-up

Exclusion criteria

Exclusion criteria: Age below 41 years and above 60 years will be excluded. Unwilling patient will be excluded. Cases having severe joints deformities like Heberden node etc. will be excluded. Cases with complications like severe ankylosed Joints and with infective joints disorders (Osteomyelitis), moderate to significant synovitis will also be excluded. Pregnant women and Lactating mothers will be excluded Patient having Rheumatoid arthritis or having Gouty arthritis will be excluded. Patient having secondary osteoarthritis (except control DM and thyroid disorder) infective or inflammatory arthritis of knee joint will be excluded. Patient have any other systemic disorder.

Design outcomes

Primary

Measure	Time frame
Reduction in pain, stiffness and improvement in joint function will be assessed in patients of Knee OsteoarthritisTimepoint: Baseline (Day 0), Day 15, Day 30, Day 45, Day 60, Day 75 and Day 90	—

Secondary

Measure	Time frame
Improvement in quality of life, joint mobility and assessment of safety and tolerability of the interventionTimepoint: Baseline, Day 15, Day 30, Day 45, Day 60, Day 75, Day 90	—

Countries

India

Contacts

Public ContactDr Rekha Bajpai

State Ayurvedic college and Hospital Tulsidas marg Tudiaganj Lucknow Uttar Pradessh

dr.rekha2101@gmail.com8004325133

Outcome results