Comparative efficacy of nasal drops and orally oil administered in neck pain.
Phase 2
- Conditions
- Health Condition 1: M479- Spondylosis, unspecified
- Registration Number
- CTRI/2023/05/052690
- Lead Sponsor
- ational Institute of Ayurveda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Patients suffering from the classical sign and symptoms of cervical spondylosis.
2)Patients of either sex between the age group of 30 to 60 years.
3)Patients willing to provide written consent and able to participate in the study for 14 days and follow up for a period of 15 days.
4)Patient fit for Nasya Karma and Snehapana.
Exclusion Criteria
1)Pregnant women and lactating mothers.
2)Patients suffering from uncontrolled systemic disorders such as Hypertension, Diabetes Mellitus and other systemic diseases which affect bones and joint conditions such as Rheumatoid arthritis.
3)Previous history of neck trauma, cervical fracture and surgery.
4)Cervical myelopathy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method