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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | culprit vessel intervention | ECG guided immediate culprit vessel intervention using a single transradial guiding catheter such as MAC or JL 3.5 |
| PROCEDURE | traditional approach | single 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.