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Trial registered on ANZCTR
Registration number
ACTRN12609000739213
Ethics application status
Approved
Date submitted
20/08/2009
Date registered
26/08/2009
Date last updated
26/08/2009
Type of registration
Prospectively registered
Titles & IDs
Public title
Spinal Modulation Neurostimulator System in the Treatment of Chronic Pain
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Scientific title
Does the Spinal Modulation Neurostimulator System provide safe and efficacious pain relief in people with chronic pain?
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Chronic Pain
243555
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Condition category
Condition code
Anaesthesiology
239857
239857
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0
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Pain management
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
This study uses an invasive neurostimulation device that is used for up to 24 hours per day. Duration of treatment in this study is 3-10 days. Part of the device is implanted in the patient and the device is controlled with a hand held remote. The amount of therapy used throughout the day is patient controlled.
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Intervention code [1]
241159
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Treatment: Devices
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Comparator / control treatment
None
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Safety as assessed by complications and adverse events. Adverse events can include increasing pain, numbness and events associated with epidural needle access. These will be assessed daily via interview and questionnaires.
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Assessment method [1]
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Timepoint [1]
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Daily assessments for 3-10 days following treatment
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Secondary outcome [1]
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Pain Relief as assessed by visual analog scale
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Assessment method [1]
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Timepoint [1]
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Daily assessments for 3-10 days following treatment
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Eligibility
Key inclusion criteria
1. Chronic pain
2. Failed conservative treatments
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Primarily axial back pain
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/09/2009
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
10
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Commercial sector/Industry
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Name [1]
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Spinal Modulation
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Address [1]
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1135 O'Brien Drive
Menlo Park, CA 94025
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Country [1]
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United States of America
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Primary sponsor type
Commercial sector/Industry
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Name
Five Corners Pty Ltd
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Address
Five Corners Pty Ltd
13/76 Reserve Road
ARTARMON NSW 2064
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
237001
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Address [1]
237001
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Country [1]
237001
0
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
The purpose of the current study is to determine the safety and efficacy of a neuromodulation therapy in the treatment of chronic pain. We hypothesize that this study will demonstrate safe delivery of therapy which will result in significant pain relief.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
30037
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Country
30037
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Phone
30037
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Fax
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Email
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Contact person for public queries
Name
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Jeff Kramer, PhD
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Address
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Spinal Modulation
1135 O'Brien Dr.
Menlo Park, CA 94025
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Country
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United States of America
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Phone
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+1 650-543-6836
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Jeff Kramer, PhD
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Address
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Spinal Modulation
1135 O'Brien Dr.
Menlo Park, CA 94025
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Country
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United States of America
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Phone
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+1 650-543-6836
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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