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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02137980

Acronym

CPORT

Enrollment

31390

Registered

2014-05-14

Start date

2011-04-01

Completion date

2016-03-31

Last updated

2018-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Angina, Coronary Artery Disease, Heart Attack

Brief 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.

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 95 Years

Healthy volunteers

Inclusion criteria

Patient inclusion criteria are: Pre-catheterization 1. must be undergoing diagnostic cardiac catheterization for suspected CAD 2. be at least 18 years of age 3. must not be pregnant (negative pregnancy test) or must not be of childbearing potential 4. must be able to give informed consent. Post-catheterization 5. coronary artery disease judged to be clinically and angiographically significant 6. ability to perform PCI with equipment available at the local site (see below) 7. procedure risk judged to be not high (see below)

Exclusion criteria

Patient

Design outcomes

Primary

Measure	Time frame
Number of participants with adverse events	Thru Index or Transfer Hospital Discharge on average 24 hours

Countries

United States

Outcome results