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A clinical study on THOKKANAM (PIDITHAL MURAI) ââ?¬â?? An external therapy using NATHAI CHOORI ENNAI (EXTERNAL) in the management of THANDAGA VATHAM (LUMBAR SPONDYLOSIS)

A open labelled clinical study to evaluate the therapeutic efficacy of THOKKANAM (PIDITHAL MURAI) ââ?¬â?? An external therapy using NATHAI CHOORI ENNAI (EXTERNAL) in the management of THANDAGA VATHAM (LUMBAR SPONDYLOSIS)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/02/031340
Enrollment
40
Registered
2021-02-16
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: M478- Other spondylosis

Interventions

Intervention1: THOKKANAM PIDITHAL MURAI (EXTERNAL) using NATHAI CHOORI ENNAI (EXTERNAL): 10-15 minutes /once a day for one week Control Intervention1: Not applicable: Not applicable

Sponsors

Government siddha medical College and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients having symptoms of Pain in the lumbar region, Radiating pain to buttocks and lower limbs, stiffness present in lumbar region, Exacerbation of pain on movements, pain increased on forward bending, tingling sensation. (Numbness) Patients who are willing to give radiological investigation and provide blood for lab investigation. Patient willing to sign the informed consent stating that he/she will conscientiously stick to the treatment during 48 days but can option out of the trail of his/her own conscious discretion.

Exclusion criteria

Exclusion criteria: Cardiac disease Auto immune diseases like Rheumatoid arthritis, SLE, Psoriasis, Mixed connective tissue disorder. Spina bifida Liver Disease Pregnancy women and lactating mother Osteo myelitis Renal Disease Tuberculosis in spine Patient with any other serious illness Other systemic illness Dislocation

Design outcomes

Primary

MeasureTime frame
Improvement in lab parameters and relief of clinical symptomsTimepoint: 48 days

Secondary

MeasureTime frame
Improvement in lab parameters and relief of clinical symptoms by using universal pain scale and clinical assessments.Timepoint: 48 days

Countries

India

Contacts

Public ContactDr G GANESAN

GOVERNMENT SIDDHA MEDICAL COLLEGE AND HOSPITAL

ganesangabriel@gmail.com9842474166

Outcome results

None listed

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