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Product Performance Report: Evaluate Long-term Reliability & Performance of Medtronic Marketed Cardiac Therapy Products
NCT00271180 · View on ClinicalTrials.gov ↗
Study Summary
The main purpose of the Product Performance Report (formerly referred to as System Longevity Study) is to evaluate long-term performance of Medtronic market-released cardiac rhythm products by analyzing product survival probabilities.
Conditions Studied
Interventions
- DEVICE Device
Study Locations (20)
California
- — Bakersfield
- — Chula Vista
- — La Jolla
- — Los Angeles
- — Palm Springs
- — Rancho Mirage
- — Redwood City
- — Salinas
- — San Diego
- — Stanford
- — Torrance
- — Van Nuys
- — Ventura
Arkansas
- — Jonesboro
- — Little Rock
Colorado
- — Aurora
- — Centennial
Alabama
- — Birmingham
Alaska
- — Anchorage
Arizona
- — Chandler
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20,000 participants |
| Start Date | 1983-01 |
| Est. Completion | 2040-12 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00271180
The ClinicalTrials.gov registry entry for NCT00271180 describes a study currently listed as recruiting. 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 20,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medtronic, 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 Heart Failure appearing as the primary indexed condition, and to 1 intervention — of which Device 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: NCT00271180 reports 20 study locations spanning 6 distinct geographic areas — top geographies include California, Arkansas, Colorado. 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 NCT00271180 about?
NCT00271180 is a clinical study titled "Product Performance Report: Evaluate Long-term Reliability & Performance of Medtronic Marketed Cardiac Therapy Products". The main purpose of the Product Performance Report (formerly referred to as System Longevity Study) is to evaluate long-term performance of Medtronic market-released cardiac rhythm products by analyzing product survival probabilities.
What is the current status of trial NCT00271180?
This trial is currently recruiting. The enrollment target is 20,000 participants. The study started on 1983-01. Estimated completion is 2040-12.
What conditions does trial NCT00271180 study?
This clinical trial studies the following conditions: Heart Failure, Bradycardia, Arrhythmia, Sinus Tachycardia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00271180?
The interventions under investigation include: Device (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00271180?
This trial is sponsored by Medtronic, 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 NCT00271180 being conducted?
This trial has 20 study locations across Alabama, Alaska, Arizona, Arkansas, California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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