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Treatment of pain in nape of the neck radiating to upper limbs in ayurvedic management

A Randomized comparative clinical study to evaluate the efficacy of Sarvamayantaka Ghrita nasya and Panchasneha Taila nasya in Vishwachi VIS A VIS Cervical Radiculopathy - NILL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087867
Enrollment
40
Registered
2025-05-29
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system

Interventions

None listed

Sponsors

Dr Pallavi Chandrakant Koli
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Subjects presenting signs and symptoms of Cervical radiculopathy like cervical region pain radiating to upper limbs with tingling sensation and numbness. 2.Subjects of all gender of age group between of 20-60 years. 3.Both freshly diagnosed and treated cases of Cervical radiculopathy will be taken for the study. Definition of fresh cases include freshly diagnosed and untreated cases of Cervical radiculopathy. Definition of Treated cases includes those cases who are already diagnosed as Cervical radiculopathy and are on treatment and who are voluntarily willing to stop the medication will be considered for the study after giving flush out period of 07 days.

Exclusion criteria

Exclusion criteria: 1.Subjects with the history of fracture of Cervical spine will be excluded. 2.Red flag sign which are indicated for surgery will be excluded (Excruciating pain, cervical lymphadenopathy, exquisite tenderness over cervical vertebrae, nausea, vomiting, dizziness, sudden loss of bowel or bladder control). 3.Subjects with uncontrolled Diabetes mellitus and Hypertension will be excluded. 4.Subjects suffering from any other systemic disorders which interferes with the course of intervention will be excluded. 5.Subjects unfit for administration of Nasya procedure will be excluded. 6.Pregnant and lactating women will be excluded.

Design outcomes

Primary

MeasureTime frame
symptomattically decrease in pain and stiffness in cervical spineTimepoint: 0th day 8th day 31st day

Secondary

MeasureTime frame
symptomatically relief in patientsTimepoint: 0th day 8th day 31st day

Countries

India

Contacts

Public ContactDr Sanjay Kumar M D

Government Ayurveda Medical College and Hospital, Mysuru

drsanjaygowda@gmail.com9986083244

Outcome results

None listed

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