A Prospective, Phase IV, Surveillance Registry Study to Evaluate the Safety of DEFINITY® in Clinical Practice
Completed · Phase 4
Conditions studied: Cardiovascular Disease
In brief
The purpose of this registry study is to gather safety information on the current clinical use of and the safety of DEFINITY®
Key facts
- Study ID
- NCT00625365
- Run by
- Lantheus Medical Imaging
- People needed
- 1060
- Starts
- 2008-02-01
- Expected to finish
- 2009-07-01
- Last updated by the study team
- 2020-11-24
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients who, in the investigator's opinion, require DEFINITY® echocardiography due to suboptimal, unenhanced images.
You may not qualify if…
- Known hypersensitivity to perflutren, DEFINITY®, or other echo contrast agent.
- Prior SAE associated with perflutren, DEFINITY®, or administration of other echo contrast agent.
Where it is running
- UCSD Medical Center — San Diego, California, United States
- Alfieri Cardiology — Newark, Delaware, United States
- Northwestern University — Chicago, Illinois, United States
- Maine Research Associates — Auburn, Maine, United States
- Park Nicolett Institute — Saint Louis Park, Minnesota, United States
- Cardiovascular Consultants, P.C. — Kansas City, Missouri, United States
- St. Louis University — St Louis, Missouri, United States
- St. Luke's-Roosevelt Hospital — New York, New York, United States
- Mt Sinai Medical Center — New York, New York, United States
- Wake Forest University Baptist Medical Center — Winston-Salem, North Carolina, United States
- Meritcare Heart Center Cardiology — Fargo, North Dakota, United States
- University of Pittsburgh — Pittsburgh, Pennsylvania, United States
- York Hospital — York, Pennsylvania, United States
- Consultants in Cardiology — Fort Worth, Texas, United States
- University of Texas Medical Center — Galveston, Texas, United States
- The Methodist DeBakey Heart Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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