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A Study of Knee Pain and the Effect of Traditional Treatments like Marma Therapy and Agnikarma

A Critical Study of Janu Sandhi and Janu Marma with evaluation of the effect of Marma Therapy and Agnikarma in Cases of Osteoarthritis of Knee Joint - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100918
Enrollment
108
Registered
2026-01-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: M170- Bilateral primary osteoarthritis of knee

Interventions

None listed

Sponsors

Banaras Hindu University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged 40 years and older who have chronic knee pain (for more than 6 months) and diagnosed with KOA according to the American College of Rheumatology (ACR) diagnostic criteria or Patients till stage 4 OA in both knees according to Kellgren Lawrence (KL) criteria will be included in the study.

Exclusion criteria

Exclusion criteria: Patients with previous knee surgery; Those who have had intraarticular injection (steroid, prolotherapy, platelet-rich plasma, etc.), Acupuncture, or physiotherapy in the last 6 months; Patients with rheumatoid arthritis or other inflammatory joint diseases, Autoimmune, and rheumatic diseases; Secondary KOA; Senile dementia Severe psychiatric and psychological disorders; Allergic skin diseases, Ulcer, or infection; Pregnant and lactating patients Patients receiving anticoagulant therapy; Hearing aids or pacemakers; Abnormal hepatic or renal dysfunction; Neuropathic pains will be excluded

Design outcomes

Primary

MeasureTime frame
change in symptoms of osteoarthritisTimepoint: change in symptoms of osteoarthritis Outcomes will be assessed at the following specific time points: Baseline (Week 0) before starting treatment Week 4 mid-treatment assessment Week 8 post-treatment / final assessment

Secondary

MeasureTime frame
reduction in WOMAC Scale and VAS scale and increase in QOL ScaleTimepoint: 60 day study with follow up every two week

Countries

India

Contacts

Public ContactDr Ashutosh Kumar Pathak

Institute of Medical Science Banaras Hindu University

drpathakbhu@gmail.com9415812548

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026