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

Use our guide to learn which trials are right for you!

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.


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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Waterford, MI
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Arlington, VA
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Azusa, CA
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Baton Rouge, LA
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Bethlehem, PA
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Bloomfield Hills, Michigan 48302
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Bloomfield Hills, MI
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Charleston, West Virginia 25304
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Charleston, WV
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Chula Vista, CA
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Durham, NC
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Edmonds, WA
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Evansville, IN
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Houston, TX
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Jacksonville, FL
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Kalispell, MT
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Kirkland, WA
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Louisville, KY
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Mansfield, OH
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Morgantown, WV
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Muncie, IN
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New York, NY
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Purcell, OK
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Sacramento, CA
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Saint Paul, MN
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San Juan,
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Scottsdale, AZ
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Southlake, TX
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Syracuse, NY
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Tampa, FL
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Utica, NY
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Webster, TX
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Williamsville, NY
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Winston-Salem, NC
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