Effect of Nebulized Dexmedetomidine on Central Sensitization and Chronification in Migraine
Condition(s) studied
Investigational drug(s) / intervention(s)
Dexmedetomidine: Assessment the effect of nebulized dexmedetomidine on central Sensitization and Chronification in patients with episodic or early chronic migraine by using CGRP serum levels and trigeminal neurophysiological biomarkers (nociceptive blink reflex (nBR) and trigeminal somatosensory evoked potentials (TSSEP)).
Study summary
Migraine is a debilitating neurological disorder characterized by recurrent headaches episodes, often accompanied by amplified perception of multiple sensory inputs such as cutaneous allodynia, photophobia, and phonophobia. The suggested mechanism in migraine is likely through sensitized trigeminovascular and dysfunctional pain modulatory systems.
Dexmedetomidine, a selective α2-adrenergic receptor agonist, exerts central antinociceptive effects by reducing neuronal hyperexcitability, glial activation, and CGRP expression. Nebulized administration provides a non-invasive alternative to intravenous use, with rapid CNS absorption and minimal sedation .
Eligibility
Primary outcome measure(s)
- Treatment of Chronic Migraine — 6 Months
Assessment of the patients whom suffering from Chronic Migraine treated by Nebulized Dexmedetomidine on Central Sensitization and Chronification in Migraine
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Beni-Suef University Hospital | Banī Suwayf | Egypt | Recruiting |
More Beni-Suef University trials in Egypt
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07769255 on ClinicalTrials.gov ↗ ← All trials in Egypt