Plain-English translation of NCT04241328 on ClinicalTrials.gov β Β· Source last updated Β· Translation generated Β· How we translate trials
This is a registry β a large database β that collects real-world safety and performance information about Medtronic cardiac surgery devices and perfusion products used during heart surgery. By gathering data from thousands of patients, researchers can spot any unexpected problems that weren't seen before, confirm that the devices work as expected, and make sure they're safe for future patients.
After a medical device is approved and used in hospitals, companies must continue watching how it performs in real patients and real conditions. This registry exists to catch any new or unexpected safety issues early, so that doctors and patients have the most up-to-date information about device safety and reliability.
You likely qualify ifβ¦
You likely don't qualify ifβ¦
Participation is simple and fits into your normal care. Your hospital will collect information about your surgery, how the device performed, and any safety events β all based on the routine care you're already receiving. You don't need to make extra visits or take on special procedures; the registry just documents what's already happening as part of your hospital treatment.
AI-generated summary from trial data Β· Jun 13, 2026 Β· Not medical advice
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