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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05399576
Other study ID # 2022-KL-085-03
Secondary ID
Status Recruiting
Phase Phase 2
First received
Last updated
Start date May 17, 2022
Est. completion date September 17, 2023

Study information

Verified date May 2022
Source The First Affiliated Hospital of Zhejiang Chinese Medical University
Contact yuangang Qiu, doctor
Phone 18069785911
Email 13957120120@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Percutaneous coronary intervention (PCI) remains the major revascularization strategy for patients with obstructive coronary artery disease (CAD).However,in a substantial number of PCI cases for acute coronary syndrome (ACS) and chronic coronary syndrome (CCS),periprocedural myocardial injury or myocardial infarction (MI) occurs,both these PCI-related complications may be associated with an increased risk of future major adverse cardiovascular events (such as death, re-infarction, and revascularization).The incidence of periprocedural myocardial injury varies according to the different definition and cardiac biomarker .For 4th UDMI criteria with hs-cTn, 78% to 85% patients who undergoing elective PCI may suffer from periprocedural myocardial injury. Experimental and clinical evidence highlight the abnormalities of the coronary microcirculation is one of the causes of myocardial ischemia.Coronary microvascular disturbances (CMD) have been associated with early stages of atherosclerosis even prior to any angiographic evidence of epicardial coronary stenosis, as well as to other cardiac pathologies such as myocardial hypertrophy and heart failure. In this study, we try to conduct a double blinded, randomized, placebo-controlled trial,the aim of our trial is: (1) to observe whether the prophylactically intracoronary administration of nicorandil and verapamil could reduce the occurrence of periprocedural myocardial injury and infarction in CAD patients undergoing elective PCI.;(2) to observe whether the prophylactically intracoronary administration of nicorandil and verapamil has protective effect on coronary microcirculation after elective PCI.


Description:

Simple randomization in a 1:1 ratio will be made in blocks of variable size according to a random numbers generated by Excel 2019 to divide the patients to treatment group (Nicorandil and verapamil) and control group (Saline). The primary end points are the incidence of periprocedural myocardial injury and 4a MI and the level of the IMR,secondary end points include levels of hs-cTnI, CK-MB ,NT-proBNP and hs-CRP before, and 24 hours following PCI, and major adverse cardiovascular events at day 30. SPSS 26.0 will be used, and P-value < .05 will be considered statistically signifificant.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date September 17, 2023
Est. primary completion date May 17, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - 1.diagnosis of CHD with FFR<0.8;2.elective PCI; Exclusion Criteria: - Patients with AMI, lesion at the opening of the main coronary artery,kidney dysfunction, Liver dysfunction,blood coagulation disorder ,NYHA III-IV,Degree II-III atrioventricular block,and restenosis after PCI,CABG will be excluded.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Nicorandil
Prophylactically combined intracoronary of Nicorandil and verapamil
Saline
intracoronary of 4ml saline

Locations

Country Name City State
China yuangang Qiu Hangzhou Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
The First Affiliated Hospital of Zhejiang Chinese Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of periprocedural myocardial injury and infarction after PCI 2.periprocedural myocardial injury was defined as hypersensitive troponin exceeding the upper limit of normal after surgery Within 24 hours after surgery
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