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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05043597
Other study ID # LHD Thrombus aspiration
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date March 1, 2020
Est. completion date February 28, 2023

Study information

Verified date September 2021
Source Shenzhen People's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study intends to evaluate thrombus on the basis of different methods for evaluating thrombus load The effect of aspiration on the prognosis of STEMI patients with high thrombotic load Provide a basis for the standardized use of aspiration; at the same time, discover the best benefit groups for thrombus aspiration


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 3838
Est. completion date February 28, 2023
Est. primary completion date January 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - (1) Age = 18 years; (2) Voluntary signing of informed consent; (3) Onset of 12 hours STEMI patients who underwent PCI reperfusion therapy within time; (4) The guidewire passes through the lesion and the blood Heavy embolism load (TIMI thrombus classification = 3). Exclusion Criteria: - (1) Hemodynamics is unstable or there is cardiogenic shock; (2) After thrombolytic therapy; (3) The expected survival time is less than 6 months due to non-cardiac diseases; (4) Past trips Coronary artery bypass graft patients; (5) Participate in other drug and device research within 30 days; (6) Before surgery, clear active gastrointestinal bleeding or other contraindications for taking dual antiplatelet drugs (7) Patients deemed unsuitable for enrollment by other researchers

Study Design


Related Conditions & MeSH terms

  • ST Elevation Myocardial Infarction
  • STEMI

Intervention

Procedure:
Thrombus aspiration
Thrombus aspiration

Locations

Country Name City State
China Shenzhen People's Hospital Shenzhen

Sponsors (1)

Lead Sponsor Collaborator
Shenzhen People's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Adverse cardiovascular events Including cardiogenic death, recurring myocardial infarction Stent thrombosis or target vessel revascularization 3 years
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