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Endothelin-1 as a Potential Trigger of Migraine Aura

Primary Purpose

Migraine With Aura

Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Endothelin-1
Placebo
Sponsored by
Glostrup University Hospital, Copenhagen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Migraine With Aura focused on measuring [C10.228.140.546.399.750.250]

Eligibility Criteria

18 Years - 40 Years (Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Danish Headache Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Endothelin-1

Placebo

Arm Description

Intravenous infusion of pharmaceutical grade human endothelin-1

Intravenous infusion of placebo (isotonic saline)

Outcomes

Primary Outcome Measures

Occurrence of migraine aura

Secondary Outcome Measures

Cerebral vasoconstriction: MR angiography
Time 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 mapping
Cerebral 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 labeling
Regional 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.

Full Information

First Posted
September 3, 2016
Last Updated
December 10, 2019
Sponsor
Glostrup University Hospital, Copenhagen
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1. Study Identification

Unique Protocol Identification Number
NCT02906085
Brief Title
Endothelin-1 as a Potential Trigger of Migraine Aura
Official Title
Investigations of the Endogenous Vasoconstrictor and Neuromodulator Peptide Endothelin-1 as a Potential Trigger of Migraine Aura
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Unknown status
Study Start Date
October 2016 (Actual)
Primary Completion Date
May 2018 (Actual)
Study Completion Date
December 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Glostrup University Hospital, Copenhagen

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Migraine With Aura
Keywords
[C10.228.140.546.399.750.250]

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Endothelin-1
Arm Type
Experimental
Arm Description
Intravenous infusion of pharmaceutical grade human endothelin-1
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Intravenous infusion of placebo (isotonic saline)
Intervention Type
Drug
Intervention Name(s)
Endothelin-1
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Isotonic saline
Primary Outcome Measure Information:
Title
Occurrence of migraine aura
Time Frame
0-24 hours
Secondary Outcome Measure Information:
Title
Cerebral vasoconstriction: MR angiography
Description
Time 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.
Time Frame
0-30
Title
Change in cerebral blood flow: Phase contrast mapping
Description
Cerebral 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.
Time Frame
0-30 minutes
Title
Change in cerebral blood flow: Arterial spin labeling
Description
Regional 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.
Time Frame
0-30 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Facility Information:
Facility Name
Danish Headache Center
City
Glostrup
ZIP/Postal Code
2600
Country
Denmark

12. IPD Sharing Statement

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Endothelin-1 as a Potential Trigger of Migraine Aura

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