To study the effect of Ayurvedic treatment in the improvements of patients with Cervical Spondylitis.
- Conditions
- Health Condition 1: M452- Ankylosing spondylitis of cervicalregion
- Registration Number
- CTRI/2023/11/060046
- Lead Sponsor
- Mprex Healthcare Pvt.Ltd. Wakad, pune
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Male and female subjects 30-60 years of age (both inclusive)
2.Subject diagnosed with cervical spondylitis with or without nerve compression for more than three months.
3.Pain in the neck and shoulder, and difficulty with neckline rotation, flexion, extension,etc.
4.Subject have Muscle spasm, Numbness, Tingling sensation, and joint stiffness.
5.Be willing to refrain from taking analgesics, anti-inflammatory agents, corticosteroids, muscle relaxants, etc. during the entire trial.
6.An ambulatory subject can provide verbal and written consent and is ready to comply with all study procedures.
1. Patients suffering from a pathological condition like a Bone tumor, Tuberculosis spine, etc.
2. History of injury to the cervical spine with the major surgical intervention will be excluded.
3. Female subjects, who are pregnant, breastfeeding, or planning to become pregnant.
4. Patients who are unable to walk without support and/or confined to a wheelchair or bedridden.
5. History of psychiatric disorder that may impair the ability of subjects to provide written informed consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. To study Panchakarma Essentials efficacy in <br/ ><br>reducing cervical spondylitis pain. <br/ ><br>2. To study the patient’s relief from stiffness & <br/ ><br>other associated symptomsTimepoint: Seven Sessions in two weeks
- Secondary Outcome Measures
Name Time Method 1. To study improvement in the Cervical Range <br/ ><br>of Movement. <br/ ><br>2. To assess the improvement in the Quality of <br/ ><br>life of a patientTimepoint: Seven Sessions in two weeks