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Clinical Trial Summary

An non controlled, long term, multi center investigation


Clinical Trial Description

Subjects who provided written informed consent and are eligible for the study will be asked to complete a daily diary for 4 weeks during the screening period. In the diary the subjects will record headache and migraine days, any changes in their health, and concomitant medications they may be using. The data collected in the diary during this screening period will be used as Baseline for the performance assessments. A non-controlled, long term, multi-center investigation for symptom improvement in subjects suffering headache and migraine attacks. During the run-in (baseline) period and through the whole study the subjects will continue using their existing prescribed or over the counter (OTC) treatments. Following the run-in period (4 weeks) the subjects will be treated six times within a period that is approximately 6 weeks. The first treatment will be given the first day after the run-in period. During 12-month follow-up period (from the time of the first treatment), subjects will be treated when needed but a maximum of 14 treatments. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05843721
Study type Interventional
Source Chordate Medical
Contact Peter J Goadsby, Prof,MD,PhD
Phone +44-20-3299 3106
Email peter.goadsby@kcl.ac.uk
Status Recruiting
Phase N/A
Start date November 8, 2023
Completion date January 15, 2025

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