MedPath

Homoeopathic treatment of neck pai

Phase 2
Conditions
Health Condition 1: M541- Radiculopathy
Registration Number
CTRI/2023/03/050202
Lead Sponsor
D N De Homoeopathic Medical College and Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1. Patients suffering from cervical radiculopathy (ICD10 CM code M54.12) for 3 months or more who shows Spurlingâ??s test positive and Bakodyâ??s sign or positive shoulder abduction test.

2. Age between 18 and 65 years

3. Participants of either sex or transgender

4. Literate participants, ability to read and write in English, Bengali and/or Hindi. Illiterate participants will be interviewed by the investigators maintaining adequate privacy to fill up the scales or questionnaires.

5. Providing with written informed consent voluntarily

Exclusion Criteria

1. Cases with complications such as incomplete neurological recoveries, disc prolapse, disc herniation.

2. Patients with the history of taking spinal steroid injection within 6 months.

3. Patients on regular NSAIDS therapy.

4. Patients with uncontrolled diabetes mellitus, uncontrolled hypertension, or uncontrolled cardiovascular disease.

5. Vulnerable population - unconscious, non-ambulatory, too sick for consultation, differently abled, terminally ill or critically ill patients, institutionalized subjects, mentally incompetent people.

6. Diagnosed cases of unstable mental or psychiatric illness or other uncontrolled or life-threatening illness affecting quality of life or any organ failure.

7. Pregnant and puerperal women, lactating mothers.

8. Patients with a habit of tobacco chewing and/or smoking, alcoholism and/or any other form(s) of substance abuse and/or dependence.

9. Self-reported immune-compromised states.

10. Already undergoing homoeopathic treatment for chronic disease within last 6 months.

11. Simultaneous participation in any other clinical trials

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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