About this trial
Last updated 13 years ago
Study ID
G060192
Status
Completed
Type
Interventional
Phase
N/A
Placebo
No
Accepting
18+ Years
All
Not accepting
Healthy Volunteers
Trial Timing
Ended 14 years ago
What is this trial about?
Clinical evaluation of the safety and efficacy of the Prometra Programmable Infusion Pump
to accurately supply drug to the intrathecal space for the treatment of chronic pain.
What are the participation requirements?
Inclusion Criteria
- suffering from chronic pain
- 18 years of age or older
- life expectancy >6 months
- failure to respond to less invasive methods
- patient undergone successful morphine trial
- patient agrees with Protocol requirements
- patient considered good subject per clinician
Exclusion Criteria
- Existing spinal problems that prevent treatment
- systemic infection
- patient is pregnant or breast feeding
- known allergy or sensitivity to materials
- coexisting medical condition that precludes pump usage
- subject requires MRI post procedure
- subject unwilling/unable to comply