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The effect of riboflavin to prevent the migraine in 5-13 year-old children

The effect of riboflavin to prevent the migraine in 5-13 year-old children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013020412361N1
Enrollment
90
Registered
2013-03-09
Start date
2013-03-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Migraine. Episodic and paroxysmal disorders

Interventions

Intervention 1: Interventional group1: Riboflavin 50mg BID for 2 months. Intervention 2: Control group: placebo(neutral drug) for 2 months. Intervention 3: Interventional groups2: Riboflavin 100mg BI
Prevention
Interventional group1: Riboflavin 50mg BID for 2 months
Control group: placebo(neutral drug) for 2 months
Interventional groups2: Riboflavin 100mg BID for 2 months

Sponsors

Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 13 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 5-13 year-old migraineous children according to ICHD II criteria who have minimally two moderate to severe migraine attacks monthly. Exclusion criteria: Epilepsy or severe neurologic disorders ; Liver, kidney, GI, metabolic or cardiovascular disorders ; Use of migraine prophylactic drugs during the last month ; Incooperation of parents or patients ; Headache attacks less than twice per month ; Tension headache ; Mild migraine headache

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Duration of headache. Timepoint: last month of treatment. Method of measurement: interview with parents and child.;Intensity of headache. Timepoint: last month of treatment. Method of measurement: interview with parents and child.;Frequency of headache attacks. Timepoint: last month of treatment. Method of measurement: interview with parents and child.

Secondary

MeasureTime frame
Urine color change. Timepoint: during the study weekly. Method of measurement: interview with parents and children.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Babak Soltani

Kashan University of Medical Sciences

babak_soltani1969@yahoo.com+98 36 1557 5840

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 7, 2026