SLIM: Effect of Sumatriptan on Levcromakalim-Induced Symptoms in Individuals With Migraine
Study Details
Study Description
Brief Summary
The study aims to explore the effects of Sumatriptan on Levcromakalim-induced migraine in individuals with migraine without aura.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| N/A |
Detailed Description
Opening of adenosine triphosphate-sensitive potassium (KATP) channels using Levcromakalim cause migraine attacks with and without aura in a high proportion of patients.
Sumatriptan has been shown to reverse Levcromakalim-induced dilation of the middle meningeal artery and headache in healthy volunteers, indicating that Sumatriptan can overturn the physiological effects of levcromakalim.
The study aims to explore the effects of Sumatriptan on Levcromakalim-induced migraine in individuals with migraine without aura.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Levcromakalim-Sumatriptan 20 participants with migraine without aura will receive a 20 min infusion of levcromakalim followed by a 10 min infusion of sumatriptan. |
Drug: Levcromakalim
20 min infusion of 1 mg Levcromakalim followed by either sumatriptan or placebo.
Drug: Sumatriptan
10 min infusion of 4 mg sumatriptan.
|
| Placebo Comparator: Levcromakalim-Placebo 20 participants with migraine without aura will receive a 20 min infusion of levcromakalim followed by a 10 min infusion of saline. |
Drug: Levcromakalim
20 min infusion of 1 mg Levcromakalim followed by either sumatriptan or placebo.
Drug: Saline
10 min infusion of isotonic saline (placebo).
|
Outcome Measures
Primary Outcome Measures
- Incidence of migraine attacks [Assessed from baseline to 12 hours after infusion of levcromakalim.]
A migraine attack is defined as an attack fulfilling either (i) or (ii): (i) Headache fulfilling criteria C and D for migraine without aura according to the International Classification of Headache Disorders 3rd edition: C. Headache has at least two of the following characteristics: unilateral location pulsating quality moderate or severe pain intensity (moderate to severe pain intensity is considered ≥4 on the numerical rating scale) aggravation by cough (in-hospital phase) or causing avoidance of routine physical activity (out-hospital phase) D. During headache at least one of the following: nausea and/or vomiting photophobia and phonophobia (ii) Headache described as mimicking the patient's usual migraine attack and treated with acute migraine medication (rescue medication).
Secondary Outcome Measures
- Incidence of headache [Assessed from baseline to 12 hours after infusion of levcromakalim.]
Incidence of headache is defined as headache intensity ≥1 as measured by a numerical rating scale (NRS) from 0 to 10. It is a verbally declared scale from 0 to 10, where 0 is no pain and 10 is the worst pain imaginable.
- Intensity of headache [Assessed from baseline to 12 hours after infusion of levcromakalim.]
Headache intensity scores are measured by a numerical rating scale (NRS). It is a verbally declared scale from 0 to 10, where 0 is no pain and 10 is the worst pain imaginable.
- Diameter of superficial temporal artery (STA) assessed using high frequency ultrasound [Assessed from baseline to 2 hours after infusion of levcromakalim.]
Diameter (mm) of superficial temporal artery (STA) is measured as a continuous outcome using high frequency ultrasound (Dermascan C, Cortex Technology, Denmark).
- Incidence of adverse events [Assessed from baseline to 12 hours after infusion of levcromakalim.]
Participants are instructed to inform the investigators in the case of adverse events.
Other Outcome Measures
- Incidence of facial flushing [Assessed from baseline to 2 hours after infusion of levcromakalim.]
Incidence of facial skin flushing assessed by the investigator as a binary outcome.
- Facial blood flow assessed using Laser Doppler Flowmetry [Assessed from baseline to 2 hours after infusion of levcromakalim.]
Facial blood flow is measured as a continuous outcome using Laser Doppler Flowmetry (LDI, Moor Instruments, Devon, United Kingdom).
- Facial temperature assessed using FLIR infrared thermal camera [Assessed from baseline to 2 hours after infusion of levcromakalim.]
Facial temperature is measured as a continuous outcome using FLIR infrared thermal camera (FLIR A655sc, Flir Systems, Sweden)
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Participant has provided informed consent prior to initiation of any study-specific activities/procedures.
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Age ≥18 years upon entry into screening.
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History of migraine without aura for ≥12 months with a frequency of 1-5 migraine attacks per month before screening according to the International Headache Society (IHS) Classification ICHD-3 (Headache Classification Committee of the International Headache Society, 2018), based on medical records and/or patient self-report.
Exclusion Criteria:
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History of any primary headache disorder other than migraine without aura, or tension-type headache with a frequency of ≥5 headache days per month before screening according to the International Headache Society (IHS) Classification ICHD-3 (Headache Classification Committee of the International Headache Society, 2018), based on medical records and/or patient self-report.
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History of any secondary headache disorder before screening according to the International Headache Society (IHS) Classification ICHD-3 (Headache Classification Committee of the International Headache Society, 2018) based on medical records and/or patient self-report.
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Any headache 48 hours prior to, or any migraine 72 hours prior to the start of the experiment on day 1 and 2.
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Daily consumption of any drug/medication other than oral contraception (birth control).
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Intake of prophylactic migraine medication within ≤30 days or 5 plasma half-lives (whichever is longer) prior to screening.
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The participant is at risk of self-harm or harm to others as evidenced by past suicidal behavior.
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History or evidence of any other clinically significant disorder, condition, or disease (with the exception of those outlined above) that, in the opinion of the investigator will pose a risk to participant safety or interfere with the study evaluation, procedures or completion.
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Female participants of childbearing potential with a positive pregnancy test assessed at screening or day 1 by a urine pregnancy test.
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Female participants who are pregnant or breastfeeding or plan to become pregnant or breastfeed during participation in the study.
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Evidence of current pregnancy or breastfeeding per participant self-report or medical records.
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Participants likely to not be available to complete all protocol-required study visits or procedures, and/or to comply with all required study procedures to the best of the participants' and investigator's knowledge.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Danish Headache Centre | Glostrup | Zealand | Denmark | 2600 |
Sponsors and Collaborators
- Danish Headache Center
Investigators
- Principal Investigator: Messoud Ashina, Prof., Danish Headache Center
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- H-21011542