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Completed

NCT Number: NCT03878784

PACAP38 Induced Headache and Rosacea-like Symptoms in Patients With Rosacea

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

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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 rosacea pathophysiology. Infusions of PACAP38 can trigger migraine-like attacks in migraine patients. PACAP38 also induces flushing which may imitate rosacea-like flushing. We are investigating whether the flushing after PACAP38 resembles rosacea-like flushing, and whether treatment with sumatriptan has an effect on the headache and flushing effects of PACAP38.

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

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • diagnosed with rosacea
  • 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

Primary outcomes

  1. Incidence of headache and migraine

    Time frame: From 0 to 24 hours after infusion

    Incidence of PACAP38-induced headache and migraine-like attacks in patients with rosacea measured by numerical rating scale for pain from 0 ("no pain") to 10 ("worst pain imaginable") and international classification for migraine.

  2. Effect of sumatriptan

    Time frame: From 0 to 24 hours after infusion

    Severity of PACAP38-induced headache after pretreatment with sumatriptan in rosacea 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

    Severity of PACAP38-induced flushing with and without sumatriptan-treatment measured by laser doppler flowmetry

  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

Sponsors and collaborators

Lead sponsor

Danish Headache Center

Other

Registry information

Official study title

Investigation of PACAP38-induced Headache and Rosacea-like Symptoms in Patients With Rosacea

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Mar 18, 2019
Registry last updated
Mar 26, 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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