CompletedNot Applicable

Registry of Non-primary Angioplasty at Hospitals Without Surgery On-site

United States31,390 participantsStarted 2011-04-01

Plain-language summary

This is a simple registry of patients undergoing PCI at hospitals without surgery on-site who were participants in the CPORT-E project. The aim of the registry is simple data collection and reporting to respective State Departments of Health. The registry population consists of patients undergoing diagnostic cardiac catheterization for suspected CAD at hospitals without SOS and who require PCI.

Who can participate

Age range18 Years – 95 Years

SexALL

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Inclusion criteria

✓. must be undergoing diagnostic cardiac catheterization for suspected CAD
✓. be at least 18 years of age
✓. must not be pregnant (negative pregnancy test) or must not be of childbearing potential
✓. must be able to give informed consent. Post-catheterization
✓. coronary artery disease judged to be clinically and angiographically significant
✓. ability to perform PCI with equipment available at the local site (see below)
✓. procedure risk judged to be not high (see below)

Exclusion criteria

✕. inability to give informed consent
✕. ST-segment elevation myocardial infarction
✕. pregnancy Post-catheterization
✕. high likelihood of requiring a device not available at the hospitals without SOS (see below)
✕. no need for PCI
✕. need for coronary artery bypass surgery
✕. high procedural risk (see below)

What they're measuring

Number of participants with adverse events

Timeframe: Thru Index or Transfer Hospital Discharge on average 24 hours

Trial details

NCT IDNCT02137980

SponsorJohns Hopkins University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2015-12-31

View on ClinicalTrials.gov More Coronary Artery Disease trials