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Investigating the effect of adding L-carnitine supplement to migraine prophylaxis treatment

Investigating the effect of adding L-carnitine supplement to migraine prophylaxis treatment on the symptoms and signs of migraine headaches.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200418047116N3
Enrollment
48
Registered
2023-09-10
Start date
2023-09-23
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Migraine. Migraine, unspecified

Interventions

Intervention 1: Intervention group: L-carnitine 500 mg tablets of Kharazmi Company are crushed and placed inside the capsule and taken once a day orally for one month to be added to the routine migrai

Sponsors

Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Signed informed consent Migraine with or without aura according to the International Classification of Headache Disorders Having 2 or more migraine attacks per month during the past 3 months Migraine onset before age 50 BMI (kg/m2) between 18 and 35

Exclusion criteria

Exclusion criteria: Absence of kidney disease or reduced kidney function and liver cirrhosis No previous use of L-carnitine No use of = 3 prophylactic medications against migraine during the past 5 years No alcohol or illegal drug addiction Not having asthma or vascular disease, arterial lameness Pregnancy, breastfeeding

Design outcomes

Primary

MeasureTime frame
Number of days with moderate to severe headache lasting more than 4 hours or treated with usual treatments. Timepoint: Before the intervention and 4 and 8 weeks after the intervention. Method of measurement: check list.

Secondary

MeasureTime frame
Number of days with migraine. Timepoint: Before the intervention and 4 and 8 weeks after the intervention. Method of measurement: check list.;Severity of headache on days with headache. Timepoint: Before the intervention and 4 and 8 weeks after the intervention. Method of measurement: MIGSEV scale.;Doses of analgesics and triptans. Timepoint: Before the intervention and 4 and 8 weeks after the intervention. Method of measurement: check list.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNegar Shafaei Bajestani

Gonabad University of Medical Sciences

negar.shafaei89@gmail.com+98 51 5723 6833

Outcome results

None listed

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