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Treatment of headache (on one side of head) with Unani medicine Capsule Shaqiqa

Phase 3
Conditions
Health Condition 1: G439- Migraine, unspecified
Registration Number
CTRI/2021/06/034390
Lead Sponsor
Central Council for Research in Unani Medicine CCRUM New Delhi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1. Patients of either gender in the age group 18- 65 years

2. Primary diagnosis of Migraine without aura by ICHD-3 beta as follows:

A. At least five attacks fulfilling criteria Bâ??D.

B. Headache attacks lasting 4-72 hours (untreated or unsuccessfully treated).

C. Headache has at least two of the following four characteristics:

Unilateral location

Pulsating quality

Moderate or severe pain intensity

Aggravation by or causing avoidance ofroutine

physical activity (e.g. walking or climbing stairs).

D. During headache at least one of the following:

1. Nausea and/or vomiting.

2. Photophobia and phonophobia.

E. Not better accounted for by another ICHD-3diagnosis.

Exclusion Criteria

1. Known case of any structural brain abnormalities

2. Known case of Ocular disease

3. History of Ischaemic stroke

4. Any disease involving sinus e.g. Rhinosinusitis

5. Systemic illness requiring long term treatment

6. Known cases of Chronic kidney & liver disease

7. Known cases of Psychiatric illness

8. Difficulty distinguishing migraine headache from other headaches

9. Known cases of Epilepsy and other neurological disorders

10. History of alcohol and drug abuse.

11. Pregnancy & lactation

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement in signs and symptoms of Shaqiqa (Migraine)Timepoint: The patients will be assessed clinically at baseline and at every two weeks till the completion of the trial i.e. upto 12 weeks
Secondary Outcome Measures
NameTimeMethod
Haematological and biochemical assessment for safety assessmentTimepoint: At baseline and at every two weeks till the completion of the trial i.e. upto 12 weeks
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