Occipital nerve stimulation in patients with medically intractable chronic cluster headache: A PET study
Completed
- Conditions
- cluster headache10019231
- Registration Number
- NL-OMON39533
- Lead Sponsor
- eids Universitair Medisch Centrum
- Brief Summary
Trial is onging in other countries
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 24
Inclusion Criteria
Participants of the ICON study
see for details ICON study protocol
Exclusion Criteria
exclusion criteria ICON study
contra indications PET scan
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary endpoint will be the difference in rCBF following 6 months of ONS<br /><br>compared to their baseline rCBF difference,</p><br>
- Secondary Outcome Measures
Name Time Method <p>The secondary endpoint is the difference in scores on subjective<br /><br>questionnaires and to explore the putative differences in rCBF between high<br /><br>(100%) stimulation and low (30%) stimulation.</p><br>