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OpenTrials
Completed

NCT Number: NCT03881644

PACAP38 Induced Headache, Migraine and Flushing in Patients With Migraine

The aim is to investigate the incidence of headache, migraine attacks and flushing after pituitary adenylate cyclase-activating peptide-38 (PACAP38) with and without treatment with sumatriptan in patients with migraine

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

DanishHC

Glostrup Municipality, DK-2600, Denmark

About this study

Pituitary adenylate cyclase-activating peptide-38 (PACAP38) plays a role in migraine pathophysiology. Infusions of PACAP38 can trigger migraine-like attacks in some migraine patients and will induce flushing in all patients. We are investigating whether treatment with sumatriptan has an effect on the PACAP38-induced flushing and on whether headache and migraine is induced.

The purpose of this study is to investigate PACAP38-induced headache and migraine in patients with migraine who have been treated with either sumatriptan or placebo using purpose-developed standardized interview. The study will be conducted with a double-blind, placebo-controlled crossover study design.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • diagnosis of migraine, according to IHS criteria
  • weight between 50 - 100 kilograms
  • women in fertile age must not be pregnant and must use adequate contraception

Exclusion criteria

  • migraine more than 5 days per month in average over the past year
  • any primary headache other than migraine, apart from tension-type headache which must be less than 5 days per month
  • headache < 48 hours before experimental day
  • migraine < 72 hours before each experimental day
  • daily / frequent use of any medication apart from contraceptive medication
  • use of any drug less than 5 times the half-life of the drug at the time of the experiment
  • women who are pregnant or breast-feeding at the time of the experiment
  • anamnestic or clinical signs of hypertension (systolic blood pressure > 150 mmHg and/or
  • diastolic blood pressure > 100 mmHg) or hypotension (systolic blood pressure < 90 mmHg and/or diastolic blood pressure < 50 mmHg)
  • anamnestic or clinical signs of mental illness, or abuse of alcohol / drugs
  • patients with glaucoma or prostate hyperplasia
  • anamnestic or clinical symptoms of any sort that the investigating doctor deemed unfit for participating in the study

Treatment and study plan

Imigran

Drug

All patients will undergo this intervention on one of two study days

Other names: Sumatriptan

Isotonic saline

Other

All patients will undergo this intervention on one of two study days

Pituitary adenylate cyclase-activating peptide-38

Other

All patients will undergo this intervention on both study days

Other names: PACAP38

Primary outcomes

  1. Incidence of migraine

    Time frame: From 0 to 12 hours after infusion

    Incidence of migraine after PACAP38-infusion will be estimated through a standardized interview based on the international headache classification for migraine

  2. Effect of Sumatriptan

    Time frame: From 0 to 12 hours after infusion

    Severity of PACAP38-induced headache and migraine after pretreatment with sumatriptan in migraine patients measured by numerical rating scale for pain from 0 ("no pain") to 10 ("worst pain imaginable")

Secondary outcomes

  1. Severity of flushing

    Time frame: From 0 to 4 hours after infusion

    Facial skin blood flow (flushing) will be measured by laser doppler flowmetry to evaluate the severity of PACAP38-induced flushing with and without sumatriptan-treatment

  2. Facial temperature

    Time frame: From 0 to 4 hours after infusion

    PACAP38-induced temperature changes with and without sumatriptan-treatment measured by infrared thermography

  3. Superficial temporal artery diameter

    Time frame: From 0 to 4 hours after infusion

    Superficial temporal artery diameter after PACAP38 with and without sumatriptan-treatment measured by ultrasound

  4. Severity of headache

    Time frame: From 0 to 12 hours after infusion

    Severity of PACAP38-induced headache will be rated on a numerical rating scale for pain from 0 ("no pain") to 10 ("worst pain imaginable")

Sponsors and collaborators

Lead sponsor

Danish Headache Center

Other

Registry information

Official study title

Investigation of PACAP38 Induced Headache, Migraine and Flushing in Patients With Migraine

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Mar 19, 2019
Registry last updated
Jun 22, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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