DyeVert™ System for Contrast Monitoring in At-Risk Patients Undergoing Angiography: A Real-World Registry
Status unconfirmed
Conditions studied: Patients at Risk for Developing Contrast-induced Nephropathy
In brief
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.
Key facts
- Study ID
- NCT03825094
- Run by
- Osprey Medical, Inc
- People needed
- 10000
- Starts
- 2019-05-07
- Expected to finish
- 2023-12-01
- Last updated by the study team
- 2022-04-18
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- DyeVert Group Patients: Patient underwent a diagnostic and/or interventional angiography procedure in which the DyeVert System was used in a majority of the case
- Patient is willing and able to provide appropriate informed consent (if required)
You may not qualify if…
- Required data was not collected or is not available
- In the Investigator or Sponsor's opinion, the patient is not considered to be suitable
Where it is running
- 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
- The University of Texas Health Science Center — San Antonio, Texas, United States
- CHRISTUS Health-Westover Hills — San Antonio, Texas, United States
- St. Mary's Medical Center — Huntington, West Virginia, United States
- West Virginia University — Morgantown, West Virginia, United States
Full record on ClinicalTrials.gov
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