Safety and Effectiveness of Spinal Cord Stimulation With Automatic Control to Treat Chronic Pain in an Extended Trial
CompletedNot applicableNCT02161627
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The aims of the study are to compare automatic control of spinal cord stimulation with manual control in patients with chronic pain of the trunk and limbs
Study details
- Official title
- Prospective, Multicenter, Randomized Double-blind Crossover Study Examining the Safety and Effectiveness of Spinal Cord Stimulation Incorporating Feedback to Treat Patients With Chronic Pain of the Trunk and/or Limbs in an Extended Trial
- Conditions
- Interventions
- Device: Saluda Medical External Trial System
- Device: Saluda Medical External Trial System
- Sponsor
- Saluda Medical Pty Ltd
- Start date
- 2014-07
- Primary completion
- 2015-05
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Countries
- United States
- Total sites listed
- 10
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: Patients enrolled in this study must meet the following inclusion criteria: 1. Have been diagnosed with chronic, intractable pain of the trunk and/or limbs (VAS ≥ 5), which has been refractory to conservative therapy for a minimum of 3 months. 2. Have been approved to undergo a trial of SCS. 3. Be an appropriate candidate for the surgical procedures required in this study based on the clinical judgment of the implanting physician 4. Be on a stable dose (no new, discontinued, or changes in dose) of all prescribed pain medication for at least 4 weeks prior to the trial 5. Be 18 years of age or older at the time of enrollment 6. Be willing and capable of giving informed consent 7. Be willing and able to comply with study-related requirements, procedures, and visits 8. Females of childbearing age must have a negative urine pregnancy test at baseline Exclusion Criteria: Patients enrolled in this study must not meet the following exclusion criteria: 1. Have a medical condition or pain in other area(s), not intended to be treated with SCS, that could interfere with study procedures, accurate pain reporting, and/or confound evaluation of study endpoints, as determined by the Investigator 2. Have evidence of an active disruptive psychological or psychiatric disorder or other known condition significant enough to impact perception of pain, compliance of intervention and/or ability to evaluate treatment outcomes 3. Are not a surgical candidate due to a diagnosis of a coagulation disorder, bleeding diathesis, progressive peripheral vascular disease or uncontrolled diabetes mellitus 4. Have a diagnosis of scoliosis that precludes lead placement 5. Have a condition, treatable with SCS, that requires leads to be inserted into the cervical region 6. Have an existing drug pump and/or SCS system or another active implantable device such as a pacemaker 7. Have a condition currently requiring or likely to require the use of MRI or diathermy 8. Have pain due to a malignant disease 9. Have a life expectancy of less than 1 year 10. Have an active systemic or local infection 11. Be allergic, or have shown hypersensitivity, to any materials of the neurostimulation system which come in contact with the body 12. Be pregnant or nursing (if female and sexually active, subject must be using a reliable form of birth control, be surgically sterile or be at least 2 years post-menopausal) 13. Have within 6 months of enrollment a significant untreated addiction to depend…
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT02161627