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An Ayurvedic Panchakarma therapy for cervical spondylosis.

Phase 2
Completed
Conditions
Health Condition 1: null- Cervical Spondylosis with clinical and radiological evidence of Cervical Spondylosis with or without cervical radiculopathy.Health Condition 2: M479- Spondylosis, unspecified
Registration Number
CTRI/2015/10/006300
Lead Sponsor
CCRAS
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
59
Inclusion Criteria

1.Cervical Spondylosis with clinical and radiological evidence of Cervical Spondylosis with or without cervical radiculopathy.

2.Willing Patients with informed consent obtained.

Exclusion Criteria

1. Age below 30 years and above 65 years.

2. Cases of cervical Spondylosis with intractable pain, neurological deficit, severe deltoid or wrist extensors weakness.

3. Patients with any cervical pathology apart from Cervical Spondylosis excluding any clinical evidence of Cervical Spondylotic myelopathy.

4. Patients with poorly controlled Hypertension ( 140/90 mmHg).

5. Patients with poorly controlled Diabetes Mellitus having HbA1C of 7.5%

6. Patients who have a past history of any type of heart disease or stoke.

7. Patients with any hepatic or renal disorder, with liver enzymes twice the normal or S. creatinine 1.4 mgm.

8. Any other condition which the Investigator thinks may jeopardize the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
â?¢Relief in Signs & Symptoms (pain and associated complaints) of the disease by â?? <br/ ><br> <br/ ><br>1. Change in the VAS score <br/ ><br>2. Change in the percentage score of Northwick Park Neck Pain Questionnaires.Timepoint: 1. Change in the VAS score from the baseline to the 14th and 21st day. <br/ ><br>2. Change in the percentage score of Northwick Park Neck Pain Questionnaires from the baseline to the 14th and 21st day.
Secondary Outcome Measures
NameTimeMethod
Improvement in health status by SF 36 QuestionnaireTimepoint: â?¢SF-36 QOL assessment for any improvement from the baseline to the 14th day.
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