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Clinical trialNCT03825094UnknownObservational

DyeVert™ System for Contrast Monitoring in At-Risk Patients Undergoing Angiography: A Real-World Registry

SponsorOsprey Medical, IncEnrollment10,000Patients at Risk for Developing Contrast-induced Nephropathy
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this registry-based study is to evaluate the ongoing, real-world clinical performance and safety of commercially available DyeVert Systems during typical clinical use for patients undergoing coronary or peripheral angiography for diagnostic and/or interventional procedures.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

  • Anand Prasad, MD, FACC

    UT Health Science Center San Antonio: Prof of Medicine & Director Cardiac Catheterization Laboratory

    Principal Investigator

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

11 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Hartford Healthcare

    Hartford, Connecticut, United States

  • Steward Palmetto General Hospital

    Hialeah, Florida, United States

  • Emory Healthcare

    Atlanta, Georgia, United States

  • Atlanta Va Medical Center

    Decatur, Georgia, United States

  • Midwest Heart & Vascular Specialists

    Overland Park, Kansas, United States

  • St. Elizabeth Healthcare

    Edgewood, Kentucky, United States

  • North Mississippi Medical Center

    Tupelo, Mississippi, United States

  • Christus Health-Westover Hills

    San Antonio, Texas, United States

  • the University of Texas Health Science Center

    San Antonio, Texas, United States

  • St. Mary'S Medical Center

    Huntington, West Virginia, United States

  • West Virginia University

    Morgantown, West Virginia, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
7 May 2019
Primary completion
31 Dec 2023
Completion
31 Dec 2023
Last update posted
18 Apr 2022
Registered enrollment
10,000
Registry id
NCT03825094

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 4 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.