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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT05868044




Registration number
NCT05868044
Ethics application status
Date submitted
2/05/2023
Date registered
22/05/2023
Date last updated
16/05/2024

Titles & IDs
Public title
REsponse to Combined SONS and ONS in Chronic Cluster headachE
Scientific title
REsponse to Combined SuPra-orbital and Occipital Nerve Stimulation in Chronic Cluster headachE With the PRIMUS System, a First in Human Study
Secondary ID [1] 0 0
SCI-01-CCH
Universal Trial Number (UTN)
Trial acronym
RESPONSE
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Chronic Cluster Headache 0 0
Condition category
Condition code
Neurological 0 0 0 0
Other neurological disorders
Musculoskeletal 0 0 0 0
Other muscular and skeletal disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Devices - PRIMUS

Experimental: PRIMUS - PRIMUS system


Treatment: Devices: PRIMUS
PRIMUS system
Intervention code [1] 0 0
Treatment: Devices
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Safety Evaluation
Timepoint [1] 0 0
4 weeks
Primary outcome [2] 0 0
Safety Evaluation
Timepoint [2] 0 0
12 months

Eligibility
Key inclusion criteria
Main

- Able and willing to provide informed consent

- Documented chronic cluster headache for at least 1 year as per ICHD-3 criteria

- Attack frequency of = 4 attacks per week for = 4 weeks before enrolment

- Documented failure of verapamil (failure meaning ineffective, provoked unacceptable
side-effects or contra-indicated)

- Stable on preventive treatment for at least two weeks prior to enrolment.

- Agree to refrain from starting new prophylactic cluster headache medication or other
preventive treatments, from 4 weeks before entering the baseline period throughout the
duration of the study

- MRI available (not older than 4 years prior to study enrolment) or willing to undergo
an MRI to exclude structural lesions potentially causing headache

- Able and willing to complete a headache Diary

Main
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
- Any other chronic primary or secondary headache disorder, unless they can clearly
differentiate them from cluster headache attacks based on the quality and associated
symptoms

- Concomitant neuromodulation, except tVNS

- Previous failure to any implantable neuromodulation device for neurovascular headache

- Have an existing Active Implantable Medical Device nearby the implant location (e.g.
DBS, cochlear implant, …)

- Metal implants in the skull (e.g. skull plates, seeds) nearby the implant

- Have a pacemaker or implantable cardioverter defibrillator (ICD)

- Suboccipital infiltrations with steroids and/or local anaesthetics or use of oral
steroids in the past 3 months

- Use of botulinum toxin injections in the past 12 weeks

- Calcitonin gene-related peptide inhibitors started less than 12 weeks prior to
enrolment

- Women of childbearing age who are pregnant, nursing or not using contraception

Study design
Purpose of the study
Device Feasibility
Allocation to intervention
N/A
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Not Applicable
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
2/05/2023
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
30/04/2026
Actual
Sample size
Target
5
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
QLD
Recruitment hospital [1] 0 0
Resolve Pain - Buderim
Recruitment postcode(s) [1] 0 0
4556 - Buderim

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Salvia BioElectronics
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
The purpose of this study is to demonstrate the safe use of the PRIMUS System in subjects
with chronic cluster headache. This is a single-centre, open label, prospective, first in
human study to collect initial clinical data on the PRIMUS system for the treatment of
chronic cluster headache.
Trial website
https://clinicaltrials.gov/ct2/show/NCT05868044
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Paul Frank, MD
Address 0 0
Resolve Pain
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Wim Pollet, MD
Address 0 0
Country 0 0
Phone 0 0
+32 498 57 98 98
Fax 0 0
Email 0 0
[email protected]
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT05868044