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Comparison of Pregabalin and Cinnarizine on treatment of children with migraine

Comparison of Pregabalin and Cinnarizine on prophylactic treatment of children with migraine

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230415057911N1
Enrollment
74
Registered
2023-05-21
Start date
2021-06-10
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Migraine. Migraine

Interventions

Intervention 1: The first intervention group: In this group, a Pregabalin oral capsule 50 mg or 75 (manufactured by Actoverco, Iran)mg was prescribed for weight of less than 30 kg and more than 30kg r

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 17 Years

Inclusion criteria

Inclusion criteria: Consent of parents and children over 13 years to participate in the study Boys and girls aged 6 to 17 years with migraine prophylaxis Migraine diagnosis based on the criteria of the International Headache Society, which includes cases of migraine without aura (5 attacks), migraine with aura (2 attacks), and each attack lasts 1 to 72 hours, and it is pulsating and severe, and accompanied by symptoms With nausea or vomiting, photophobia, phonophobia Not taking pregabalin and cinnarizine in the past

Exclusion criteria

Exclusion criteria: Drug Intolerance (symptoms such as diarrhea, nausea and vomiting) anaphylaxis severe dizziness excessive sleepiness

Design outcomes

Primary

MeasureTime frame
Frequency of migraine headaches. Timepoint: The beginning of the study, 4, 8 and 12 weeks after the intervention. Method of measurement: Patient's history and notes.

Secondary

MeasureTime frame
Severity of migraine headaches. Timepoint: The beginning of the study, 4, 8 and 12 weeks after the intervention. Method of measurement: Based on the Visual Analogue Scale (VAS).;The rate of migraine attacks disability. Timepoint: The beginning of the study, 4, 8 and 12 weeks after the intervention. Method of measurement: Based on Pediatric Migraine Disability Assessment (PedMIDAS) tool.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Vafaeeshahi

Iran University of Medical Sciences

vafaeeshahi.m@iums.ac.ir+98 21 2304 6253

Outcome results

None listed

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