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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
The Walton Center
Liverpool
L97LJ
Cluster Headache
Monitor the safety and performance of the Pulsante Microstimulator System.
The recruitment start and end dates are as follows:
Apr 2015
May 2018
You can take part if:
Inclusion Criteria:
1. Patient meets CE marked labeling for cluster headache.
2. Patient has the ability to read, comprehend and reliably record information as required by the Protocol.
3. Patient is able to provide written informed consent prior to participation in the study.
Exclusion Criteria:
1. Patient has other significant pain problem that might confound the study assessments in the opinion of the Investigator.
You may not be able to take part if:
This is in the inclusion criteria above
Below are the locations for where you can take part in the trial.
The study is sponsored by Autonomic Technologies, Inc. .
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
for Trial ID: NCT02440776
The information is provided by researchers and we rely on them to keep it up-to-date. You can see more information by clicking on the 'Read full details' link above.
To take part, please print or share the study information with your GP/healthcare provider or contact the research team directly.