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A study on sathakuppai ottradam (fomentation) for cervical spondylosis patients

An open clinical evaluation of Sathakuppai ottradam (Sathakuppai fomentation) in the Management of Sagana vaatham (Cervical spondylosis) – Phase II clinical trail - Nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068879
Enrollment
100
Registered
2024-06-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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: Sathakuppai ottradam: Therapy Duration 15 days. Once in a day.Total Study duration 12 months Control Intervention1: Nil: Nil

Sponsors

Government Siddha Medical College, Chennai
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pain present in the cervical region radiating to the back of the head, top of the shoulders, shoulder blades, upper arms and hands. Neck stiffness and Difficulty in flexion, extension and lateral rotation of neck, Numbness and paraesthesia of neck or shoulders or upper limbs, Neck Disability Index score should be equal or greater than 40%, Shoulder abduction pain relief sign – positive Lhermitte’s sign and Spurling’s sign – positive Chin chest test - positive

Exclusion criteria

Exclusion criteria: Known case of Traumatic injury Tuberculosis of bone Extra cervical rib Pyogenic bone infection Vertebral fracture Tumour in vertebral body Pregnant women and lactating mothers.

Design outcomes

Primary

MeasureTime frame
Reduction in pain is assessed by Visual Analogue Scale (VAS) and Neck Disability Index (NDI). Improvement in range of movements is assessed by ROM evaluation chart.Timepoint: 12 months

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactDr M Kannan

Government Siddha Medical College, Arumbakkam, Chennai-106.

vmkkannan2020@gmail.com9444216514

Outcome results

None listed

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