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Implantable Systems Performance Registry
NCT00959296 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- DEVICE Various
Study Locations (20)
California
- — Aliso Viejo
- — Los Angeles
- — Napa
- — Palm Springs
- — Pasadena
- — San Diego
- — Upland
Florida
- Site recruiting for sacral nerve stimulation — Bradenton
- — Merritt Island
- — Ocala
Indiana
- — Evansville
- — Muncie
- — South Bend
Georgia
- — Atlanta
- — Gainesville
Illinois
- — Bloomington
- — Chicago
Alabama
- — Huntsville
Arizona
- — Scottsdale
District of Columbia
- — Washington D.C.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10,981 participants |
| Start Date | 2003-08 |
| Est. Completion | 2016-09-27 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00959296
The ClinicalTrials.gov registry entry for NCT00959296 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 10,981 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is MedtronicNeuro, which has 14 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 4 conditions, with Deep Brain Stimulation appearing as the primary indexed condition, and to 1 intervention — of which Various is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00959296 reports 20 study locations spanning 8 distinct geographic areas — top geographies include California, Florida, Indiana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00959296 about?
NCT00959296 is a clinical study titled "Implantable Systems Performance Registry". 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 ava...
What is the current status of trial NCT00959296?
This trial is currently completed. The enrollment target is 10,981 participants. The study started on 2003-08. Estimated completion is 2016-09-27.
What conditions does trial NCT00959296 study?
This clinical trial studies the following conditions: Deep Brain Stimulation, Spinal Cord Stimulation, Drug Infusion (Implantable Pumps), Sacral Neuromodulation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00959296?
The interventions under investigation include: Various (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00959296?
This trial is sponsored by MedtronicNeuro, which has 14 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00959296 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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