A Prospective Clinical Outcomes Registry
Status: | Completed |
---|---|
Conditions: | Chronic Pain |
Therapuetic Areas: | Musculoskeletal |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/1/2019 |
Start Date: | June 2009 |
End Date: | April 2014 |
Partnership for Advancement In Neuromodulation (PAIN): A Prospective Clinical Outcomes Registry
This is a prospective non-interventional 24 month post implant registry. Any patient that
receives a St. Jude Medical FDA approved implantable neuromodulation system is eligible for
enrollment. A minimum of 600 patients will be enrolled from a minimum of 30 sites.
Patients will be enrolled post-implant and followed for 24 months. Data are collected at
enrollment (within 30 days of device implant), and routine care follow-up visits at 3 months,
6 months, 12 months, 18 months and 24 months.
receives a St. Jude Medical FDA approved implantable neuromodulation system is eligible for
enrollment. A minimum of 600 patients will be enrolled from a minimum of 30 sites.
Patients will be enrolled post-implant and followed for 24 months. Data are collected at
enrollment (within 30 days of device implant), and routine care follow-up visits at 3 months,
6 months, 12 months, 18 months and 24 months.
Inclusion Criteria:
1. Patient has signed and received a copy of the Informed Consent form;
2. Patient has been implanted with a St. Jude Medical Neuromodulation system, including
battery and/or SCS leads;
3. Patient is 18 years of age or older.
4. Patient is not currently participating in another clinical trial.
Exclusion Criteria:
We found this trial at
32
sites
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