Rigshospitalet-Glostrup
Glostrup Municipality, 2600, Denmark
Location status: Recruiting
Location contact
Haidar Al-Khazali, MD
CONTACT
Haidar Al-Khazali, MD
SUB_INVESTIGATOR
Hakan Ashina, MD, PhD
CONTACT
NCT Number: NCT07059546
Adrenomedullin is a neuropeptide implicated in the pathogenesis of headache. This study investigates whether adrenomedullin induces headache with migraine-like features in people with persistent post-traumatic headache (PTH) attributed to mild traumatic brain injury (mTBI).
Interested in participating?
Request Info18 year–65 year
All sexes
Interventional
Not applicable
Glostrup Municipality, 2600, Denmark
Location status: Recruiting
Haidar Al-Khazali, MD
CONTACT
Haidar Al-Khazali, MD
SUB_INVESTIGATOR
Hakan Ashina, MD, PhD
CONTACT
Adrenomedullin is a potent vasoactive peptide that acts on the vascular smooth muscle and is known to induce vasodilation. It is endogenously expressed in the trigeminovascular system, a key anatomical substrate involved in headache pathogenesis. Evidence suggests that individuals with persistent post-traumatic headache (PTH) frequently experience headache with migraine-like symptoms. This study investigates whether intravenous infusion of adrenomedullin can provoke migraine-like headache in individuals with persistent PTH attributed to mild traumatic brain injury. To test this hypothesis, the investigators will carry out a randomized, double-blind, placebo-controlled, two-way crossover trial.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The participants will receive continuous intravenous infusion of 20 mL of 19.9 pmol/kg/min adrenomedullin over 20 minutes.
The participants will receive a continuous intravenous infusion of 20 mL of placebo (isotonic saline) over 20 minutes.
Time frame: 12 hours
The difference in incidence of headache with migraine-like features between adrenomedullin and placebo during the 12-hour observational period after infusion start.
Time frame: 12 hours
The secondary outcome is the difference in the area under the curve (AUC) for headache intensity scores between adrenomedullin and placebo during the 12-hour observational period after infusion start.
Contact information is provided by the study sponsor or research team.
Haidar Al-Khazali, MD
CONTACT
Hakan Ashina, MD,PhD
CONTACT
Danish Headache Center
Other
Hypersensitivity to Adrenomedullin in Post- Traumatic Headache: A Randomized Clinical Trial
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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