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NCT03272451
ECG-guided Immediate Primary PCI for Culprit Vessel to Reduce Door to Device Time
NA trial testing culprit vessel intervention in Myocardial Infarction in 560 participants. Completed in 31 July 2019.
15 July 2019
Quick facts
| Lead sponsor | Beijing Luhe Hospital |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 560 |
| Start date | 10 February 2017 |
| Primary completion | 15 July 2019 |
| Estimated completion | 31 July 2019 |
| Sites | 2 locations across China |
Drugs / interventions tested
- culprit vessel intervention
- traditional approach
Conditions studied
- Myocardial Infarction — all drugs for Myocardial Infarction →
Sponsor
Beijing Luhe Hospital
Who can join
18 and older, any sex, with Myocardial Infarction. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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).
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Culprit vessel revascularization first with primary use of a dedicated transradial guiding catheter to reduce door to balloon time in primary percutaneous coronary intervention.
Guo J, Wang G, Li Z, Liu Z, et al · · 2022 · cited 4× · PMID 36386357 · DOI 10.3389/fcvm.2022.1022488
Verify or expand the search:
- PubMed search for NCT03272451
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Beijing Luhe Hospital trials
Trials by the same sponsor.
- NCT06364124 — Effects of PCSK-9 Inhibitor Treatment Prior to Undergoing Primary Percutaneous Coronary Intervention in Patients With ST · NA · recruiting
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- NCT04078451 — Study of Left Side of Laparoscopic Cholecystectomy · NA · unknown
- NCT05266547 — Impact of OCT on Outcomes in AMI · unknown
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03272451 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Beijing Luhe Hospital
- Last refreshed: 1 June 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03272451.
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