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Determination of the therapeutic efficacy of ginger in the treatment of migraine headaches

Phase 3
Conditions
Migraine.
Migraine
Registration Number
IRCT20220818055740N2
Lead Sponsor
Shahre-kord University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
80
Inclusion Criteria

Age between 18 to 65 years; history of migraine headache before performing the study based on IHS criteria; headache from moderate to severe less than six days by visual analogue score(Vas); absence of diseases such as liver, heart, active stomach ulcer, diabetes and renal failure.

Exclusion Criteria

Abnormal vital signs during the study;, new abnormal findings during CT scan; dissatisfaction patients to continue the study;, and observation of drug sensitivity.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Migraine headache. Timepoint: One month after intervention. Method of measurement: VAS, PSQI, MIDAS questionnaires.
Secondary Outcome Measures
NameTimeMethod
Migraine headache. Timepoint: One month after intervention. Method of measurement: VAS, PSQI, MIDAS questionnaires.
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