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Endothelin-1 as a Potential Trigger of Migraine Aura

Investigations of the Endogenous Vasoconstrictor and Neuromodulator Peptide Endothelin-1 as a Potential Trigger of Migraine Aura

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02906085
Enrollment
60
Registered
2016-09-19
Start date
2016-10-31
Completion date
2019-12-31
Last updated
2019-12-12

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

Conditions

Migraine With Aura

Keywords

[C10.228.140.546.399.750.250]

Brief summary

One third of migraine patients experience aura, i.e. dramatic, transient neurological symptoms, most often in the form of visual disturbances, that usually appear before the onset of migraine headache. The likely underlying mechanism of aura is known as cortical spreading depression, a wave of changes in electrical activity that slowly spreads in the outermost layer of the brain. It is currently not known what causes the aura to initiate in patients or what the relationship is between aura and migraine headache, e.g. if treatment targeted at aura mechanisms will prevent subsequent headache. Due to the short-lasting and unpredictable nature of aura, the only possible approach for systematic investigations is to experimentally trigger aura, but currently no method for aura-triggering is available. The overall goal of the proposed project is to reveal the earliest mechanisms of the migraine attack by investigating the initiating factors of aura in the migraine brain. Current animal evidence indicates that infusion of endothelin-1 (ET-1), a naturally occurring signaling molecule released from blood vessels, is safe and very likely to trigger migraine aura in patients. In this project the investigators aim to study the effects of ET-1 on the human brain, to investigate aura-inducing effects of ET-1 in patients and to develop a safe and reliable method for the experimental induction of migraine aura using ET-1.

Interventions

DRUGPlacebo

Isotonic saline

Sponsors

Glostrup University Hospital, Copenhagen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Age between 18 and 40 years * Diagnosis of migraine with typical aura (patient group only) * Attacks of migraine with aura at least once per month on average (patient group only) * No history or family history of migraine (healthy subject group only) * Use of safe contraception (women of fertile age only)

Exclusion criteria

* Tension-type headache more than one day per month on average * Any other primary headache disorder * Daily intake of medication * Daily smoking during the past 5 years * Pregnant or breastfeeding women * Hypertension on the experimental day (systolic BP\>150 mmHg or diastolic BP\> 100 mmHg) * History of any cardiovascular disease including cerebrovascular disease * History of diabetes or hypercholesterolemia * ECG changes suggestive of ischemia * Contraindications of MRI

Design outcomes

Primary

MeasureTime frame
Occurrence of migraine aura0-24 hours

Secondary

MeasureTime frameDescription
Cerebral vasoconstriction: MR angiography0-30Time of flight arteriography using 3 tesla MRI (healthy subjects). Arterial diameters and circumferences (mm) will be measured from the resulting angiography images. This type of investigation will be carried out in healthy subjects only.
Change in cerebral blood flow: Phase contrast mapping0-30 minutesCerebral blood flow (perfusion, ml/100 g/min) measured before and after intervention using MRI phase contrast mapping (measure of global brain perfusion). This type of investigation will be carried out in healthy subjects only.
Change in cerebral blood flow: Arterial spin labeling0-30 minutesRegional cerebral blood flow (perfusion, ml/100g/min) measured before and after intervention using MRI pseudo-continous arterial spin labelling at 3 tesla. This type of investigation will be carried out in healthy subjects only.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026