Skip to content

Establishment of predictors and predictive models of no-reflow after primary percutaneous coronary intervention in STEMI patients

Establishment of predictors and predictive models of no-reflow after primary percutaneous coronary intervention in STEMI patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900026390
Enrollment
Unknown
Registered
2019-10-07
Start date
2020-01-01
Completion date
Unknown
Last updated
2019-10-14

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

Conditions

ST-segment elevation myocardial infarction

Interventions

Index test:predictors&#32
and&#32
predictive&#32
of&#32
no-reflow

Sponsors

Affiliated Hospital of Guilin Medical College
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. STEMI was treated by primary PCI; 2. Patients agreed to participate in the clinical study and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. myocardial infarction was caused by interruption of blood flow after invasive surgery, and STEMI was caused by non arteriosclerotic coronary blood flow interruption; 2. peripheral vascular disease, chronic heart failure and thyroid disease caused by major injuries in nearly six months; 3. combined with endocarditis, valvular disease, congestive heart failure and other cardiovascular diseases; 4. patients with cardiogenic shock admitted to hospital; 5. Patients with severe abnormalities in liver and kidney function; 6. patients with acute and chronic bacterial and/or viral infections or connective tissue diseases; 7. patients with diabetes mellitus, 7 patients with poorly controlled hypertension (systolic pressure > 160 mmHg or diastolic pressure > 105 mmHg) and those who used nitrate within 24 hours before admission; 8. patients with any hematological diseases, including anemia; 9. patients with any autoimmune disease; 10. patients with acetyl-free water; Anyone with antiplatelet drugs other than salicylic acid, anticoagulants or steroids; 11. clinicians did not consider them suitable for this study.

Design outcomes

Primary

MeasureTime frame
High-sensitivity C-reactive protein;ET-1;MMP-9;BNP;miR-126;miR-30e;Liver function, renal function and coagulation function;TXA2;PCT;miR-155;SEN, SPE, PPV, NPV, ACC, AUC of ROC;

Countries

China

Contacts

Public ContactQiang Su

Anesthesiology Department, Affiliated Hospital of Guilin Medical College

suqiang1983@glmc.edu.cn+86 13707715913

Outcome results

None listed

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