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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.

Contact Information:

Study Location:

The Walton Center
Liverpool
L97LJ


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Pathway CH S&E Registry

Not Recruiting

Open to: All Genders

Age: 18 Years - N/A

Medical Conditions

Cluster Headache


Study summary

Monitor the safety and performance of the Pulsante Microstimulator System.


Key dates

The recruitment start and end dates are as follows:

Apr 2015

May 2018

Study type

Observational [Patient Registry]

Who can take part?

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


Where can I take part?

Below are the locations for where you can take part in the trial.

  • The Walton Center
    Liverpool
    L97LJ

Funders/Sponsors


The study is sponsored by Autonomic Technologies, Inc. .



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for Trial ID: NCT02440776

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This page is to help you find out about a research study and if you may be able to take part

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To take part, please print or share the study information with your GP/healthcare provider or contact the research team directly.