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Effect of Predefined Homoeopathic Medicines in Cervical Spondylosis Pain Management.

Phase 2
Conditions
Health Condition 1: null- Pain due to Cervical spondylosis
Registration Number
CTRI/2011/12/002270
Lead Sponsor
Central Council for Research in Homoeopathy
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
140
Inclusion Criteria

?Patients with chief complaint of neck pain including pain in suboccipital and interscapular

region within 2 weeks.

?One or more episodes of neck pain, neck stiffness attack on average per month for at least

3 months.

?Positive radiological findings for cervical spondylosis.

?VAS score for pain is minimum 4.

?Patient not on anti inflammatory or other therapy in the past 1week known to affect the

study outcome.

Exclusion Criteria

?Cervical myelopathy or radiculopathy.

?Patient with neck pain and normal x-ray Cervical spine.

?Patients on physiotherapy.

?Having neck trauma/ fracture/ surgery history/ congenital spinal abnormalities.

?Any systemic diseases of bones and joints.

?Other non-specific neck pain lesions?acute neck strain, postural neck ache, or whiplash.

?Suffering from any systemic diseases such as hypertension, diabetes mellitus, Cardio/ Cerebro-vascular diseases etc.

?Inability to comply with the study protocol, alcoholics, drug users including psychiatric diseases.

?Pregnant and lactating women.

?Patients deemed ineligible by the investigators.

?Patient unwilling to sign the written informed consent form.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual Analogue ScaleTimepoint: Assessment of pain from Visual analogue scale shall be done daily for 7 days
Secondary Outcome Measures
NameTimeMethod
?To assess the changes in CSPMS. <br/ ><br>?To assess the rating of Patient and Clinical Global Impression (CGI) scale. <br/ ><br>Timepoint: CSPMS and Assessment of the quality of life of patients with Patient and Clinical Global Impression (CGI) scale shall be filled up on the 3rd and 8th day of the study period.
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