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Ayurvedic treatment for neck pain

Comparative study of agnikarma to evaluate the efficacy of lauha shalaka and tamra shalaka in the management of sandhigata vata w.s.r. to cervical spondylosis

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/04/008374
Enrollment
40
Registered
2017-04-19
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: null- Cervical spondylosis

Interventions

Intervention1: Agnikarma by lauha shalaka: bindu type of agnikarma on most tender points of neck region. two sitting of agnikarma with the gap of 15 days. two follow up in 30 days with gap of 15 days

Sponsors

harish daga
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients fulfilling the diagnostic criteria. Patients between the ages of 40 â?? 70 years.

Exclusion criteria

Exclusion criteria: Pregnant/lactating woman. Age below 40 years and above 70 years. Patients suffering from pathological condition like Bone tumor, Tuberculosis spine etc. Uncontrolled diabetes mellitus. History of injury to cervical spine. Who are not ready to sign written informed consent form.

Design outcomes

Primary

MeasureTime frame
Reduction in visual analouge scale(VAS) & stiffness and improvement in range of motion with in 15 days after two sittings of agnikarma.Timepoint: Reduction in visual analouge scale(VAS) & stiffness and improvement in range of motion with in 15 days after two sittings of agnikarma.

Secondary

MeasureTime frame
Improvement in headache,vertigo, loss of sensation,after two sittings of agnikarma in 15 days intervelTimepoint: Improvement in headache,vertigo, loss of sensation,after two sittings of agnikarma in 15 days intervel

Countries

India

Contacts

Public ContactHarish Daga

Parul group of institute

hemant.toshikhane@paruluniversity.ac.in8469496525

Outcome results

None listed

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