Embrace TDD: Post-Market Study to Evaluate Intrathecal Morphine as an Alternative to Systemic Opioids for Chronic Pain
Purpose
This is a prospective, multi-center, post market study to evaluate Intrathecal (IT) preservative-free morphine sulfate (PFMS) using the SynchroMed™ II infusion system as an alternative to systemic opioids for the treatment of chronic, intractable, non-malignant primary back pain with or without leg pain.
Conditions
- Chronic Non-malignant Pain
- Chronic Pain
- Pain, Back
- Pain, Leg
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Willing and able to provide a signed and dated (Medtronic and Institutional Review Board (IRB) approved) Informed Consent Form (ICF) and Health Insurance Portability and Accountability Act (HIPAA) Authorization Form prior to any study procedures being performed 2. A candidate per labeling for the Intrathecal Drug Delivery System (IDDS) 3. A diagnosis of chronic, intractable, non-malignant primary back pain with or without leg pain, treatable with the IDDS 4. Current daily systemic opioid dose of >0 and ≤ 120 Morphine Milligram Equivalents (MME) 5. A Visual Analogue Scale (VAS) of ≥50 mm for pain intensity at the Baseline Visit and/or a Numerical Opioid Side Effect (NOSE) Assessment Tool ≥40 for intolerable side effects at the Baseline Visit 6. Psychological evaluation or investigator assessment of patient psychological suitability for study participation 7. Has an MRI or CT prior to enrollment verifying patent spinal canal and no clinical change in status since last imaging 8. At least 18 years old at time of enrollment 9. Willing and able to attend visits and comply with the study protocol 10. Male or non-pregnant, non-lactating female. Females must be post-menopausal or surgically sterile; or be utilizing a medically acceptable form of birth control (i.e. a hormonal contraceptive, intra-uterine device, diaphragm with spermicide, or condom with spermicide) for the duration of the study
Exclusion Criteria
- Previously trialed or implanted with an IDDS 2. Concomitant stimulation device implanted for the treatment of pain 3. Any ongoing health condition that would be expected to interfere with pain and/or quality of life ratings (i.e. active malignancy, other painful conditions not treatable with IT therapy, etc.) 4. Psychological or other health conditions, financial and/or legal concerns that would interfere with the subject's ability to fulfill the requirements of the protocol as per the investigator's discretion 5. Substance Use Disorder (SUD) within the last 2 years or current Medication Assisted Treatment (MAT) for substance use disorder 6. Currently using cannabinoids or illicit drugs 7. History of allergy or significant adverse reaction to morphine per investigator discretion 8. Currently participating or plans to participate in another investigational study unless written approval is provided by Medtronic Study Team
Study Design
- Phase
- Phase 4
- Study Type
- Interventional
- Allocation
- N/A
- Intervention Model
- Single Group Assignment
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Other Intrathecal Therapy |
Enrolled subjects who successfully wean from all systemic opioids and have a successful intrathecal trial, proceed to the intervention phase. This includes implantation with a SynchroMed™ II infusion system in the intrathecal space for targeted drug delivery of preservative-free morphine sulfate (PFMS). |
|
More Details
- Status
- Completed
- Sponsor
- MedtronicNeuro
Study Contact
Detailed Description
Subjects will be assessed for pain control and opioid-related side effects following a route of delivery change from systemic opioids to IT morphine therapy.