To study the effect of Ayurvedic treatment in the improvements of patients with Cervical Spondylitis.

Not yet recruiting

Brief Summary: Cervical spondylosis is a general term affecting the spinal disc in the neck. The inter-vertebral spaces are affected most and start at the degeneration of discs resulting in a reduction of inter-vertebral disc space. It develops restricted cervical spine movement in the neck due to pain and swelling. The study aims to assess the Safety and Efficacy of classical Ayurvedic treatment in the functional improvements of patients with Cervical Spondylitis. The therapeutic effect is assessed by comparing relief from stiffness and other associated symptoms. Adverse effects reported by patients during treatment will be recorded.

Recruitment & Eligibility

Inclusion Criteria

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.

Exclusion Criteria

Patients suffering from a pathological condition like a Bone tumor, Tuberculosis spine, etc.
History of injury to the cervical spine with the major surgical intervention will be excluded.
Female subjects, who are pregnant, breastfeeding, or planning to become pregnant.
Patients who are unable to walk without support and/or confined to a wheelchair or bedridden.
History of psychiatric disorder that may impair the ability of subjects to provide written informed consent.

Primary Outcome Measures

Name	Time	Method
other associated symptoms	Seven Sessions in two weeks
1. To study Panchakarma Essentials efficacy in	Seven Sessions in two weeks
reducing cervical spondylitis pain.	Seven Sessions in two weeks
2. To study the patientâ€™s relief from stiffness &	Seven Sessions in two weeks

Secondary Outcome Measures

Name	Time	Method
1. To study improvement in the Cervical Range	of Movement.

Locations (1): Lokmanya Medical Research Centre
🇮🇳
Pune, MAHARASHTRA, India
Lokmanya Medical Research Centre
🇮🇳Pune, MAHARASHTRA, India
Dr Amol Gothwad
Principal investigator
9766400243
dr.amolgothwad001@gmail.com