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Agnikarma in Neck Pain

Development of Software Based Agnikarma Device in The Management of Griva Sandhigata Vata

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/02/031552
Enrollment
101
Registered
2021-02-25
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: M15-M19- Osteoarthritis

Interventions

None listed

Sponsors

Parul University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient Suffering From Neck Pain of Restricted Range of Motion of Cervical Spine or Stiffness in Neck

Exclusion criteria

Exclusion criteria: Pregnant and lactating woman Patients group of age below 25 and above 70 Patients suffering from pathological condition like Bone tumor Tuberculosis spine Uncontrolled diabetes mellitus History of injury to cervical spine Who are not ready to sign written informed consent form

Design outcomes

Primary

MeasureTime frame
patient will be improved in neck pain after agnikarma procedureTimepoint: Patients will be follow up after 15 days

Secondary

MeasureTime frame
Along With Neck Pain Patient may be Improved in Restricted Range of Motion of Cervical spine and Stiffness of Neck AlsoTimepoint: 2 week

Countries

India

Contacts

Public ContactDr Harish Daga

Parul University

drhemantt@gmail.com8469496525

Outcome results

None listed

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