Clinical Trials Directory

Trials / Completed

CompletedNCT03272451

ECG-guided Immediate Primary PCI for Culprit Vessel to Reduce Door to Device Time

ECG-guided Immediate pRimAry Percutaneous Coronary Intervention for Culprit Vessel Using a Transradial Single Guiding Catheter to Reduce Door to Device Time: RAPID II Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
560 (actual)
Sponsor
Beijing Luhe Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

No consensus exists about which coronary artery should be firstly catheterized in primary percutaneous coronary intervention (PCI). The aim of the present study was to compare door-to-balloon time (D2B) of ECG guided immediate infarct-related artery (IRA) PCI with traditional complete coronary angiography followed by PCI for the treatment of ST segment elevation myocardial infarction (STEMI) patients. Primary endpoint is door to device (D2D) time. Secondary end-points are: puncture to device (P2D) time,first medical contact to device (FMC2D) time,incidence of radial artery spasm and occlusion, contrast amount, fluoroscopy time, cumulative air kerma(CAK) and dose area product(DAP).

Conditions

Interventions

TypeNameDescription
PROCEDUREculprit vessel interventionECG guided immediate culprit vessel intervention using a single transradial guiding catheter such as MAC or JL 3.5
PROCEDUREtraditional approachsingle diagnostic catheter for complete coronary angiography and guiding catheter selection for PCI

Timeline

Start date
2017-02-10
Primary completion
2019-07-15
Completion
2019-07-31
First posted
2017-09-05
Last updated
2022-06-01

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT03272451. Inclusion in this directory is not an endorsement.