Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING

Abbott Vascular Medical Device Registry

NCT04573660 · View on ClinicalTrials.gov ↗

Study Summary

The AV-MDR is a prospective, non-randomized, open-label, multi-center registry. The purpose of the AV-MDR study is to proactively collect and evaluate clinical data on the usage of the devices in scope within their intended use with the aim of confirming safety and performance throughout their expected lifetime, ensuring the continued acceptability of identified risks, detecting emerging risks on the basis of factual evidence, ensuring the continued acceptability of the benefit-risk ratio, and identifying possible systematic misuse or off-label usage such that the intended use can be verified as appropriate.

Interventions

  • DEVICE Coronary and peripheral stents
  • DEVICE Pacing catheters
  • DEVICE Vascular plugs
  • DEVICE Measurement and imaging (FFR and OCT)
  • DEVICE Peripheral dilatation catheters

Study Locations (20)

WAUS

  • Perth Institute of Vascular Research — Nedlands
  • Sir Charles Gairdner Hospital — Nedlands

Eflndrs

  • Onze-Lieve-Vrouwziekenhuis Campus Aalst — Aalst
  • AZ Sint-Blasius Ziekenhuis — Dendermonde

Zhejian

  • Jinhua Municipal Central Hospital — Jinhua
  • Ningbo First Hospital — Ningbo

Alabama

  • University Hospital - Univ. of Alabama at Birmingham (UAB) — Birmingham

Arkansas

  • Arkansas Heart Hospital — Little Rock

California

  • Kaiser Permanente Los Angeles Medical Center — Los Angeles

Illinois

  • Northwestern Memorial Hospital — Chicago

Nebraska

  • Bryan Heart — Lincoln

Trial Details

FieldValue
Enrollment Target 3,784 participants
Start Date 2020-10-25
Est. Completion 2031-11

Sponsor

Abbott Medical Devices

155 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04573660

The ClinicalTrials.gov registry entry for NCT04573660 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 3,784 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbott Medical Devices, which has 155 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Acute Myocardial Infarction appearing as the primary indexed condition, and to 5 interventions — of which Coronary and peripheral stents 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: NCT04573660 reports 20 study locations spanning 17 distinct geographic areas — top geographies include WAUS, Eflndrs, Zhejian. 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 NCT04573660 about?

NCT04573660 is a clinical study titled "Abbott Vascular Medical Device Registry". The AV-MDR is a prospective, non-randomized, open-label, multi-center registry. The purpose of the AV-MDR study is to proactively collect and evaluate clinical data on the usage of the devices in scope within their intended use with the aim of confirming safety and performance throughout their expec...

What is the current status of trial NCT04573660?

This trial is currently recruiting. The enrollment target is 3,784 participants. The study started on 2020-10-25. Estimated completion is 2031-11.

What conditions does trial NCT04573660 study?

This clinical trial studies the following conditions: Acute Myocardial Infarction, Venous Embolism, Restenoses, Coronary, Coronary Artery Lesions, Arterial Embolism. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04573660?

The interventions under investigation include: Coronary and peripheral stents (DEVICE), Pacing catheters (DEVICE), Vascular plugs (DEVICE), Measurement and imaging (FFR and OCT) (DEVICE), Peripheral dilatation catheters (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04573660?

This trial is sponsored by Abbott Medical Devices, which has 155 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04573660 being conducted?

This trial has 20 study locations across Alabama, Arkansas, California, Illinois, Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial