Health Condition 1: M478- Other spondylosis
Conditions
Interventions
None listed
Sponsors
Dr Anushree H M
Eligibility
Inclusion criteria
Inclusion criteria: 1. Subjects with classical signs and symptoms of Manyastambha vis-a-vis Cervical spondylosis. 2. Subjects between the age group of 21-50 years. 3. Subjects of either gender irrespective of religion and socio-economic status. 4. Subjects fit for Avapeedana Nasya. 5. Subjects fit for Sthanika Nadi Sweda. 6. Subjects who are willing to give written consent and participate in the study.
Exclusion criteria
Exclusion criteria: 1. Pregnant and lactating women. 2. Subjects on concurrent medications. 3. Subjects with congenital deformity, traumatic injury, cervical stenosis and myelopathy, infections of bone and gross bony deformity and epistaxis. 4. Other systemic disorders which interfere in the line of treatment like uncontrolled diabetes, uncontrolled hypertension and cardiovascular diseases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Significant reduction in Pain, stiffness and improvement in Cervical range of movements measured by VAS scale, Stiffness grading and goniometer readings respectively. Timepoint: Trial period: 7 days Assessment on: 0th day, 7th day, 14th day Follow up: 14th day Total study duration: 14 days | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Generation of data on possible unexpected/adverse drug reactions or events. 2. Generation of data on quality of life with the test treatment modalities assessed based on Neck disability index. Timepoint: Trial period: 7 days Assessment on: 0th day, 7th day, 14th day Follow up: 14th day Total study duration: 14 days | — |
Countries
India
Contacts
Public ContactDr Ganesh Puttur
Sri Sri College Of Ayurvedic Science and Research Hospital
Outcome results
None listed