Implantable Systems Performance Registry
Status: | Completed |
---|---|
Conditions: | Hospital, Orthopedic, Psychiatric |
Therapuetic Areas: | Psychiatry / Psychology, Orthopedics / Podiatry, Other |
Healthy: | No |
Age Range: | Any |
Updated: | 4/22/2017 |
Start Date: | August 2003 |
End Date: | September 27, 2016 |
The Implantable Systems Performance Registry (ISPR) was developed to evaluate the long-term
reliability and performance of market-released Medtronic Neuromodulation infusion and
stimulation products.
Completion Notice: The ISPR was created by Medtronic to monitor the performance of
commercially available products. This registry was initially designed to track performance
of Medtronic's implantable infusion and spinal cord stimulation systems beginning in August
2003 and June 2004, respectively. Medtronic DBS Systems were added to the ISPR in June 2009,
and Sacral Neuromodulation Systems in April 2010. Medtronic retired the ISPR in April 2016
and merged the data collected from this registry into the Product Surveillance Registry
(PSR). Please refer to that record, Clinical Trials identifier: NCT01524276, for further
information.
reliability and performance of market-released Medtronic Neuromodulation infusion and
stimulation products.
Completion Notice: The ISPR was created by Medtronic to monitor the performance of
commercially available products. This registry was initially designed to track performance
of Medtronic's implantable infusion and spinal cord stimulation systems beginning in August
2003 and June 2004, respectively. Medtronic DBS Systems were added to the ISPR in June 2009,
and Sacral Neuromodulation Systems in April 2010. Medtronic retired the ISPR in April 2016
and merged the data collected from this registry into the Product Surveillance Registry
(PSR). Please refer to that record, Clinical Trials identifier: NCT01524276, for further
information.
Inclusion Criteria:
- Scheduled for an implant or replacement with a market-released Medtronic implantable
drug pump, spinal cord stimulator, deep brain stimulator, or sacral nerve stimulator
Exclusion Criteria:
- Patient who is or will be inaccessible for follow-up at an ISPR study site
- Patient is currently enrolled in or plans to enroll in any concurrent drug and/or
device study that may confound the results of this study
We found this trial at
44
sites
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Washington, D.C., District of Columbia
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