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To study the effects of ayurvedic treatment in the management of Cervical spondylosis

Phase 2
Conditions
Health Condition 1: M478- Other spondylosisHealth Condition 2: M478- Other spondylosis
Registration Number
CTRI/2024/01/061218
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.The patients having clinical signs and symptoms of Greeva Sandhigata Vata (Cervical Spondylosis). Pain must be an essential feature among all the features.

2.History of neck pain longer than 3 months.

3.The patients having chronicity of disease less than 5 years.

Exclusion Criteria

1.History of neck trauma and fracture.

2.Recent cervical, spinal, or shoulder surgery or implanted instrumentation or previous surgery for cervical spondylotic myelopathy.

3.Known case of Intravertebral disc prolapse.

4.Patient participated in any clinical trial within last six months.

5.Known case of Inflammatory arthritic conditions like Rheumatoid arthritis, Ankylosing spondylitis and Malignancy, Tuberculosis ,HIV infection.

6.Patients who are having allergy to any trial drug.

7.Pregnant or lactating women

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Changes in Visual Analogue Scale Pain score [change from pre- intervention to 2 weeks] <br/ ><br> Visual Analogue Scale pain score will be used to assess neck pain. Score ranges from 0-10. 0- shows least pain & 10- shows worst pain. <br/ ><br>Timepoint: 14 days
Secondary Outcome Measures
NameTimeMethod
1.Changes in Universal Goniometer readings from pre-intervention baseline value at the end of 2 weeks <br/ ><br>2.Changes in Neck Disability Index score from pre-intervention baseline value at the end of 2 weeks <br/ ><br>Timepoint: 30 days
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