Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07342296

Induction of Migraine Attacks With Aura Using Pituitary Adenylate Cyclase Activating Polypeptide-38

Induction of Migraine Attacks With Aura Using Pituitary Adenylate Cyclase Activating Polypeptide-38: A Randomized Clinical Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
21 (estimated)
Sponsor
Danish Headache Center · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Pituitary Adenylate Cyclase Activating Polypeptide-38 (PACAP-38) is a key neuropeptide in migraine pathophysiology and treatment. This study investigates whether PACAP-38 administration can trigger aura in individuals with a diagnosis of migraine with aura.

Detailed description

In a series of studies, pharmacological triggers of migraine headache were able to induce aura as well migraine headache. Recent open-label findings show that calcitonin gene-related peptide (CGRP) can trigger aura attacks-despite its limited ability to cross the blood-brain barrier. This suggests CGRP might induce migraine aura via trigeminovascular activation, the same pathway involved in migraine headache. To further explore this concept, it is fundamental to examine whether other migraine-inducing signaling molecules that pass the BBB to a minimal degree, such as PACAP-38, are able to induce aura as well. If PACAP-38 is able to induce aura, the anti-PACAP monoclonal antibody may provide a promising therapeutic option for preventing migraine with aura. To validate this effect, a randomized, double-blind, placebo-controlled trial is essential. Its outcomes could inform future therapies targeting the migraine-aura connection.

Conditions

Interventions

TypeNameDescription
DRUGPituitary Adenylate Cyclase Activating Polypeptide-38 (PACAP-38)The participants will receive a continuous intravenous infusion of 10 pmol/kg/min PACAP-38 over 20 min
DRUGPlaceboThe participants will receive a continuous intravenous infusion of 20 mL of placebo (isotonic saline) over 20 minutes.

Timeline

Start date
2026-02-01
Primary completion
2026-12-01
Completion
2026-12-30
First posted
2026-01-15
Last updated
2026-01-15

Source: ClinicalTrials.gov record NCT07342296. Inclusion in this directory is not an endorsement.