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KODUVELI NEI AND VARMAM THERAPY IN THE MANAGEMENT OF THANDAGA VAATHAM (LUMBAR SPONDYLOSIS) - PRE-CLINICAL AND CLINICAL STUDY

EVALUATION OF THE THERAPEUTIC EFFECTIVENESS OF KODUVELI NEI AND VARMAM THERAPY IN THE MANAGEMENT OF THANDAGA VAATHAM (LUMBAR SPONDYLOSIS) - PRE-CLINICAL AND CLINICAL STUDY - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/086153
Enrollment
138
Registered
2025-05-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: M479- Spondylosis, unspecified

Interventions

Intervention1: Koduveli nei and Varmam therapy: Koduveli Nei will be given internally foe 9 days. 3 days of drug holiday followed by it 15 days Varmam therapy Control Intervention1: Varmam therapy: Va

Sponsors

National Institute of Siddha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients having two or more clinical symptoms I.Pain in the lumbar region and pain increased in forward bending II.Radiating pain to buttocks and lower limbs III.Stiffness in the lumbar region IV.Increase in the pain on movements V.Numbness (Tingling sensation) in the lower limbs Grade I & II in the radiological findings of lumbar spine Patient who are willing to involve in the study by signing the consent and fulfilling the condition of performa, who are willing to undergo radiological and blood investigations. Patient who has Oswestry low back disability questionnaire total score 5-34

Exclusion criteria

Exclusion criteria: K/C/O Cardiovascular disease. K/C/O Autoimmune disease K/C/O spinal deformities K/C/O of renal diseases K/C/O Tuberculosis and other infections in the spine H/O Acute trauma/fracture Pregnancy and lactating mothers Patients with any other serious systemic illness.

Design outcomes

Primary

MeasureTime frame
The treatment is considered as effective by the reduction of 9 points in the score measured using Oswestry Lowback Disability Scale.Timepoint:

Secondary

MeasureTime frame
To estimate the effectiveness of drug and Varmam therapy in reducing the clinical symptoms in groups 1 and 2 compared with Standard control (Group 3) The adverse reactions will be noted in the Adverse Drug reaction form and reported to the Pharmacovigilance wing in the hospital. Timepoint:

Countries

India

Contacts

Public ContactDr M V Mahadevan

National Institute of Siddha

mvmresearch2008@gmail.com9789633690

Outcome results

None listed

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