Head Pain Clinical Trial
Official title:
Quantitative Sensory Testing, Blink Reflex and Nociceptive Flexion Reflex in the Pathophysiology of Headache
Verified date | September 2020 |
Source | University of Liege |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The aim of this study is to compare central and peripheric sensitization in headache patients at Baseline (T0) and 1 month after (T1) a treatment with an anti-CGRP (Fremanezumab-Ajovy).
Status | Not yet recruiting |
Enrollment | 40 |
Est. completion date | October 2021 |
Est. primary completion date | October 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: patients with headache which are about to receive a treatment with
fremanezumab Exclusion Criteria: - medication changes 1 month prior to the test - neuropathy - acute or chronic pain - medications having effects on the central nervous system - other disease |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Liege |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | modulation of pain threshold by fremanezumab | quantitative analysis of pain-related reflexes with QST (quantitative sensory testing) using Medoc Pathway | one year | |
Primary | modulation of pain threshold by fremanezumab | Blink reflex and nociceptive flexion reflex usig EMG Viking Viasys. | one year |
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