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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05103813
Other study ID # Beraprost Sodium treat STEMI
Secondary ID
Status Recruiting
Phase Early Phase 1
First received
Last updated
Start date May 1, 2022
Est. completion date June 30, 2023

Study information

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

Clinical Trial Summary

Protective effect of Beraprost Sodium Tablets on coronary microcirculation function and ventricular remodeling after reperfusion therapy for acute ST segment elevation myocardial infarction


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date June 30, 2023
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - It meets the diagnostic criteria of acute ST segment elevation myocardial infarction: ischemic chest pain lasts for more than 30 minutes and can not be relieved by taking nitroglycerin; ST segment elevation of ECG with two or more adjacent leads, limb lead = 1mm, chest lead = 2mm; Or new left bundle branch block; The serum markers of myocardial necrosis increased at least twice the normal value - Acute myocardial infarction was confirmed by coronary angiography - The clinical and angiographic data were complete - Direct PCI was performed within 12 hours after onset Exclusion Criteria: - Those who do not cooperate in the inspection, have poor compliance and cannot guarantee the completion of the test - Conscious disorder, obvious intellectual disorder and mental disorder - With metal foreign bodies, such as metal prosthesis, intraocular metal foreign bodies, intracranial aneurysm clamp, etc - People with claustrophobia - Had a history of myocardial infarction, PCI and coronary artery bypass grafting - Factors affecting ST segment changes of ECG: complete left bundle branch block, preexcitation syndrome, pacemaker ECG, etc

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Beraprost Sodium Tablets
Protective effect of Beraprost Sodium Tablets on coronary microcirculation function and ventricular remodeling after reperfusion therapy for acute ST segment elevation myocardial infarction

Locations

Country Name City State
China Shenzhen People' S Hospital Shenzhen Guangdong

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 Major Adverse Cardiovascular Events The incidence of mace after 1 week of treatment 1 weeks after baseline
Primary Major Adverse Cardiovascular Events The incidence of mace after 6 months of treatment 6 months after baseline
Primary Major Adverse Cardiovascular Events The incidence of mace after 1 year of treatment 1 year after baseline
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