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Effect of constipation treatment versus control group on migraine headaches in children with concurrent functional constipatio

Phase 2
Recruiting
Conditions
Migraine
Migraine.
Registration Number
IRCT20120215009014N361
Lead Sponsor
Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
100
Inclusion Criteria

Age of 4 to 15 years,
Migraine headaches with concurrent functional constipation,

Exclusion Criteria

Contraindication of propranolol (asthma, liver disease, diabetes, bradycardia, heart block),
Severe hypotension

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Rectal impaction. Timepoint: Daily for 5 days. Method of measurement: With digital rectal exam.
Secondary Outcome Measures
NameTimeMethod
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