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Effect of cinnarizine in control of pediatric migraine

Comparison of propranolol plus cinarizine and propranolol plus placebo in control of migraine headaches in children attending Imam Reza clinic in Shiraz.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180724040576N1
Enrollment
106
Registered
2018-11-08
Start date
2018-11-22
Completion date
Unknown
Last updated
2019-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric migraine. Migraine

Interventions

Intervention group: Cinnarizine(37.5 mg for children 4-11 years of age and 50 mg for children 12-16 years of age, once daily) and Propranolol (1 mg /kg body weight, once daily). Duration of treatment

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 14 Years

Inclusion criteria

Inclusion criteria: Every child with a diagnosis of migraine (according to international headache society) There must be at least 4 episodes of migraine attacks per month. The age range of 6 to 14 years. A migraine headache with or without aura. The patient has not used any drug for preventing migraine headaches during last month Parents agreement and sign informed written consent form.

Exclusion criteria

Exclusion criteria: The patient affected by other forms of migraine headache (variant migraine). The patient has focal neurologic signs or radiologic findings in brain imaging. There is a serious comorbidity. There are other systemic diseases. Inability to participate in the study. Use of drugs for preventing attacks during last month A contraindication to use of cinnarizine or propranolol (such as asthma or heart block).

Design outcomes

Primary

MeasureTime frame
Frequency of migraine headaches. Timepoint: Before intervention and 2,4,8 weeks after intervention. Method of measurement: Frequency of headaches will be recorded daily by the parents in a timetable.;Severity of migraine headaches. Timepoint: Before intervention and 2,4,8 weeks after intervention. Method of measurement: Severity of headaches will be measured by Visual Analog Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPegah Katibeh

Shiraz University of Medical Sciences

katibeh_p@sums.ac.ir+98 71 3212 7522

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026