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A Comparative study on cauterization and internal medicine Arumuga Chenduram in management of Osteoarthritis

A COMPARATIVE CLINICAL TRAIL ON THERAPEUTIC EFFICACY OF SUTTIGAI(CAUTERIZATION) AND ARUMUGA CHENDURAM (INTERNAL MEDICINE) IN THE MANAGEMENT OF AZHAL KEEL VAYU (OSTEOARTHRITIS OF KNEE)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/05/019141
Enrollment
60
Registered
2019-05-15
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: M179- Osteoarthritis of knee, unspecified

Interventions

Intervention1: Suttigai(Cauterization): 4 Sittings in 2 weeks interval Control Intervention1: Arumuga chenduram: 130 mg twice a day with Trikadugu chooranam, Honey for 45 days

Sponsors

Ayothidoss Pandithar hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients suffering from primary osteoarthritis of knee joint.Signs and symptoms of Pain, tenderness, stiffness and crepitus in kneejoint. Patients willing to undergo radiological investigation (X RAY KNEE JOINT) and Laboratory investigations. Patients willing to sign the informed consent stating that he/she will Conscientiously stick to the treatment during 48 days but can opt out of the trial of his/her own conscious discretion.Patients willing to take photograph before and after suttigai therapy

Exclusion criteria

Exclusion criteria: Recent history of trauma, fracture , surgery of affected knee joint. Presence of local infection or skin disease on the proposed site of Suttigai.H/o Cardiac diseases,Uncontrolled Diabetes mellitus,Uncontrolled Hypertension, Rheumatoid arthritis, Chronic kidney disease, Pregnancy and lactation, Secondary OA due to tuberculosis(TB), syphilis, AIDS, leprosy, Septic arthritis, Gonococcal arthritis,Psoriatic arthritis. Patient with any other serious systemic illness.

Design outcomes

Primary

MeasureTime frame
Primary outcome of the study is relieving pain and it will be assessed by KOOS KNEE SURVEY -Knee injury and Osteoarthritis Outcome Score (KOOS)- Before and after the treatment Timepoint: 45 days

Secondary

MeasureTime frame
Secondary outcome is assessed by comparing the clinical symptoms, clinical lab parameters and their quality of life before and after the treatment.Timepoint: 45 days

Countries

India

Contacts

Public ContactDr Keerthika

The tamilnadu Dr M G R Medical university

rvmahalakshmi85@gmail.com9940668576

Outcome results

None listed

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