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The effectiveness of no reflow prevention algorithm during primary percutaneous coronary intervention for acute st-segment elevation myocardial infarction

The effectiveness of no reflow prevention algorithm during primary percutaneous coronary intervention for acute st-segment elevation myocardial infarction

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000028758
Enrollment
Unknown
Registered
2020-01-02
Start date
2020-04-01
Completion date
Unknown
Last updated
2020-01-06

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

Conditions

acute st-segment elevation myocardial infarction

Interventions

algorithm group:The balloon does not dilate after passing through the occluded vessel
algorithm group:Do not perform intra-coronary instrumentation and wait 10 minutes

Sponsors

Chengdu Fifth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. It was consistent with acute st-segment elevation myocardial infarction and did not exceed the window period (onset to admission to the catheterization room <12 hours); 2. Coronary angiography TIMI flow level 0-1; 3. Agree and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with acute st-segment elevation myocardial infarction, but beyond the window period, accompanied by cardiogenic shock, third-degree atrioventricular block and other emergency PCI; 2. Acute non-st elevation myocardial infarction; 3. Chronic coronary artery occlusion; 4. It was consistent with acute st-segment elevation myocardial infarction, but the blood flow of coronary angiography TIMI was grade 2 or above; 5. PCI after thrombolytic failure; 6. There was no blood flow after the balloon first passed; 7. It is difficult for the balloon to pass through, and only by tunneling the balloon can it pass through; 8. Acute occlusion of the left main; 9. The thrombus is difficult to extract, and the catheter needs extention catheter to extract the thrombus.

Design outcomes

Primary

MeasureTime frame
Coronary TIMI grading;

Secondary

MeasureTime frame
Cardiovascular event;

Countries

China

Contacts

Public ContactLiu Zhao Hui

Chengdu Fifth people's hospital

47044356@qq.com+86 028 3458003688

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026