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Personalized CRT - PSR
NCT03723265 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate the cardiac resynchronization therapy (CRT) response in a real-world patient population and evaluate options to address non-response and patient management.
Conditions Studied
Interventions
- DEVICE Cardiac Resynchronization Therapy
Study Locations (20)
California
- — Bakersfield
- — Chula Vista
- — Palm Springs
- — Rancho Mirage
- — Redwood City
- — Salinas
- — San Diego
- — Stanford
- — Torrance
- — Van Nuys
Arkansas
- — Jonesboro
- — Little Rock
Colorado
- — Denver
- — Lakewood
Alabama
- — Birmingham
Alaska
- — Anchorage
Arizona
- — Gilbert
Connecticut
- — New Haven
District of Columbia
- — Washington D.C.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,517 participants |
| Start Date | 2012-01 |
| Est. Completion | 2022-04-28 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03723265
The ClinicalTrials.gov registry entry for NCT03723265 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 1,517 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 1 condition, with Heart Failure appearing as the primary indexed condition, and to 1 intervention — of which Cardiac Resynchronization Therapy 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: NCT03723265 reports 20 study locations spanning 9 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 NCT03723265 about?
NCT03723265 is a clinical study titled "Personalized CRT - PSR". The purpose of this study is to evaluate the cardiac resynchronization therapy (CRT) response in a real-world patient population and evaluate options to address non-response and patient management.
What is the current status of trial NCT03723265?
This trial is currently completed. The enrollment target is 1,517 participants. The study started on 2012-01. Estimated completion is 2022-04-28.
What conditions does trial NCT03723265 study?
This clinical trial studies the following conditions: Heart Failure. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03723265?
The interventions under investigation include: Cardiac Resynchronization Therapy (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03723265?
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 NCT03723265 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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