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Comparing Homoeopathic Potencies Effective in the Treatment of Cervical Spondylosis

Phase 4
Conditions
Health Condition 1: M478- Other spondylosis
Registration Number
CTRI/2024/02/062779
Lead Sponsor
Sahaana Srikumar
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients having symptomatology of cervical spondylosis.

Exclusion Criteria

1. Age below 30 and above 80 years. 2. Cases in which surgical intervention becomes necessary. 3. Patients with other co-morbidities. 4. Patients under allopathic medication for cervical spondylosis.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement of pain of cervical spondylosis is validated by using Neck Pain <br/ ><br>Disability Index. Disappearance of symptoms of the patient is assessed by using static physician global <br/ ><br>assessment score. <br/ ><br>Comparison of the effectiveness of centesimal and LM potencies will be done.Timepoint: 3 months
Secondary Outcome Measures
NameTimeMethod
Pain of the patient with cervical spondylosis will be improved with intervention & changes will be recorded & assessed using Neck Pain disability index.Timepoint: 2 weeks
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