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NCT Number: NCT06959004

Substance P-Induced Migraine Attacks Without Aura

Substance P is a neuropeptide implicated in the pathogenesis of headache. This study investigates whether its administration can trigger migraine attacks in individuals with migraine without aura.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Substance P is a vasoactive neuropeptide of the tachykinin family, expressed in various cell types, including primary afferents of the trigeminal ganglion that innervate the meninges and associated vasculature. Its most well-established role is in nociceptive signaling, and accumulating evidence implicates substance P in the pathogenesis of headache. This study investigates whether intravenous infusion of substance P can induce migraine attacks in individuals with a history of migraine without aura. To test this, the investigators will conduct a randomized, double-blind, placebo-controlled, two-way crossover trial.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 18 to 65 years of age upon entry into screening
  • A body weight of 50 to 100 kg
  • History of migraine without aura for ≥12 months and in accordance with ICHD-3
  • Between 1-5 monthly migraine days without aura on average across the 3 months prior to screening

Exclusion criteria

  • Any history of a primary or secondary headache disorder other than migraine without aura and infrequent episodic tension-type headache
  • Any history of moderate to severe traumatic brain injury
  • Any history of cardiovascular disease, including cerebrovascular diseases
  • Any history of pulmonary disease
  • Any other clinically significant disorders, conditions, or diseases that might impact the safety of the subject or interfere with the study's evaluation, procedures, or completion, aside from those mentioned above. This includes any relevant medical history or evidence that, in the opinion of the site investigator, might pose a risk to the subject or impact the validity of the study results
  • The subject is at risk of self-harm or harm to others as evidenced by past suicidal behavior
  • Female subjects of childbearing potential with a positive pregnancy test during any study visit
  • Cardiovascular disease of any kind, including cerebrovascular diseases
  • Hypertension (systolic blood pressure of ≥150 mmHg and/or diastolic blood pressure of ≥100 mmHg) prior to the start of infusion on the experimental day
  • Hypotension (systolic blood pressure of ≤90 mmHg and/or diastolic blood pressure of ≤50 mmHg)
  • Daily use of any medication other than contraceptives
  • Intake of any medication other than contraceptives within 48 hours of infusion start
  • Headache of any intensity within 48 hours of infusion start
  • Migraine attack within 5 days of infusion start
  • Aura within 48 hours of infusion start

Treatment and study plan

Substance P

Drug

The participants will receive a continuous intravenous infusion of 20 mL of substance P (4.0 pmol/kg/min) over 20 minutes.

Placebo

Drug

The participants will receive a continuous intravenous infusion of 20 mL of placebo (isotonic saline) over 20 minutes.

Primary outcomes

  1. Incidence of migraine attacks without aura

    Time frame: 12 hours

    The difference in the incidence of migraine attacks without aura between substance P and placebo during the 12-hour observational period after infusion start.

Secondary outcomes

  1. Headache intensity scores

    Time frame: 12 hours

    The secondary outcome is the difference in the area under the curve (AUC) for headache intensity scores between substance P and placebo during the 12-hour observational period after infusion start.

Study contacts

Contact information is provided by the study sponsor or research team.

Haidar Al-Khazali, MD

CONTACT

[email protected]

+4541598494

Hakan Ashina, MD, PhD

CONTACT

[email protected]

+4528102495

Sponsors and collaborators

Lead sponsor

Danish Headache Center

Other

Registry information

Official study title

Substance P-Induced Migraine Attacks Without Aura: A Randomized Clinical Trial

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
May 6, 2025
Registry last updated
Jun 5, 2025

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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