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Role of oral Coenzyme Q supplementation in children with migraine

Not Applicable
Conditions
Health Condition 1: G439- Migraine, unspecified
Registration Number
CTRI/2020/07/026271
Lead Sponsor
ICMR
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Children with age 6-18 years

2.Newly diagnosed to have migraine with/without aura

3.Not received any medication for migraine prophylaxis in the past three months

4.Caregivers giving informed consent

Exclusion Criteria

1.Already on other prophylactic treatment for migraine

2.Receiving any antioxidant/other herbal medication/nutraceuticals in the past three months

3.Any major systemic illnessAny other associated neurological disorder

4.Abnormality in neuroimaging (MRI brain/CT brain)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Comparison of the reduction in the number of headache days per month at baseline for the 3 months prior to study initiation as compared to the last 4 weeks of treatment in both arms. It will be determined by reviewing the headache diary maintained by the patient and caregivers.Timepoint: 24 weeks
Secondary Outcome Measures
NameTimeMethod
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