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Efficacy of Intracoronary Infusion of Different Medicine in STEMI Patients Undergoing Primary PCI

Efficacy of Intracoronary Infusion of Different Medicine With Targeted Perfusion Catheter on Myocardial Perfusion in Patients With STEMI Undergoing Primary PCI:an Open,Prospective,Randomized,Multicenter Trial.

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03252665
Enrollment
600
Registered
2017-08-17
Start date
2017-09-01
Completion date
2019-06-30
Last updated
2017-08-17

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

Keywords

STEMI, myocardial perfusion, TMPFC, Nicorandil, Alprostadil

Brief summary

The study intends to evaluate the efficacy of different medicine delivering by targed perfusion catheter incoronary administration on epicardial, myocardial perfusion and clinical outcomes in STEMI patients undergoing primary PCI.

Detailed description

The goal of STEMI therapy is to successfully restore both epicardial blood flow and myocardial perfusion. PCI has been documented as being the most effective method for restoration of epicardial blood flow. However, epicardial blood flow does not necessarily equate to myocardial perfusion; not every patient with TIMI 3 flow after successful PCI achieves effective myocardial tissue-level perfusion. Although epicardial TIMI 3 flow could be restored in \>90% of STEMI patients undergoing PCI, normalization of myocardial perfusion was achieved less frequently, with detrimental impacts on survival。 Currently, there are two main methods of angiographic assessment of myocardial perfusion: TIMI myocardial perfusion grading (TMPG), described by Gibson et al. and myocardial blush grading (MBG), described by Van't Hof et al. These established myocardial perfusion parameters, TMPG and MBG, have been widely used in various important trials and are reported to be highly useful in predicting clinical outcomes. However, visual assessment of these methods is categorical, subjective, and operator dependent. TIMI Myocardial Perfusion Frame Count (TMPFC), a novel and objective method that measures the filling and clearance of contrast in the myocardium using cine-angiographic frame-counting, was developed by our center to quantify myocardial tissue- level perfusion and was proved to be a predictive value on clinical prognosis. Currently, there are two main types of interventions to improve myocardial perfusion . One kind is the mechanical method, which included thrombus aspiration catheter and the distal protective devices. It has been confirmed that the mechanical method can effectively improve epicardial and myocardial perfusion in patient with part of large vessels and high burden thrombus. But for patients with small vessels and no obvious visual thrombus, the efficacy is not significant. The other kind intervention is medicine which included GP IIb/IIIa receptor antagonist , adenosine , sodium nitroprusside, verapamil etc. Part of the drugs have some effect but the overall clinical efficacy is still not satisfied. The study intends to use targeted perfusion catheter to deliver drug to the distal targeted blood vessels. TMPFC and TMPG are applied to evaluate the efficacy of treatment with Nicorandil versus Alprostadil on myocardial tissue-level perfusion in STEMI patients undergoing primary PCI.

Interventions

alprostadil,2ug, dilivered by targeted perfusion catheter in the culprit vessel after PCI in STEMI patients

DRUGNicorandil

Nicorandil,2mg, dilivered by targeted perfusion catheter in the culprit vessel after PCI in STEMI patients

DRUGNitroglycerin

Nitroglycerin,200ug, dilivered by targeted perfusion catheter in the culprit vessel after PCI in STEMI patients

Sponsors

Shanghai 10th People's Hospital
CollaboratorOTHER
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
CollaboratorOTHER
Shanghai 6th People's Hospital
CollaboratorOTHER
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
CollaboratorOTHER
Ruijin Hospital
CollaboratorOTHER
RenJi Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age: over 18 or 18 years old, less than 75 years old; * Patents with myocardial infarction who have symptom onset within 6h before randomization; * ECG: ≥2 mm ST-segment elevation in 2 contiguous precordial leads or ≥1 mm ST-segment elevation in 2 contiguous extremity leads ; * Signed informed consent form prior to trial participation.

Exclusion criteria

1. Evidence of cardiac rupture; 2. ECG: new left bundle branch block; 3. Thrombolysis contradictions: 4. Severe complication * Other diseases with life expectancy ≤12 months; * Any history of Severe renal or hepatic dysfunction(hepatic failure, cirrhosis, portal hypertension and active hepatitis); Neutropenia, thrombocytopenia ; Known acute pancreatitis; * Known acute pericarditis and/or subacute bacterial endocarditis; * Arterial aneurysm, arterial/venous malformation and aorta dissection; 5. Complex heart condition * Cardiogenic shock(SBP \<90 mmHg after fluid infusion or SBP\<100 mmHg after vasoactive drugs); * PCI within previous 1 month or Previous coronary-artery bypass surgery(CABG); * Previously known multivessel coronary artery disease not suitable for revascularization; * Hospitalisation for cardiac reason within past 48 hours; 6. Not suitable for clinical trial * Inclusion in another clinical trial; * Previous enrolment in this study or treatment with an investigational drug or device under another study protocol in the past 7 days; * Pregnancy or lactating; * Body weight \<40kg or \>125kg; * Known hypersensitivity to any drug that may appear in the study; * Inability to follow the protocol and comply with follow-up requirements or any other reason that the investigator feels would place the patient at increased risk.

Design outcomes

Primary

MeasureTime frameDescription
TIMI Myocardial Perfusion Grade (TMPG)One mins after PCITMPG is an angiographic measure of myocardial perfusion
TIMI Myocardial Perfusion Frame Count (TMPFC)One mins after PCITMPFC is a novel method to standardize and quantify myocardial perfusion by timing the filling and washout of contrast in the myocardium using cine-angiographic frame-counting. Briefly, the first frame of TMPFC was defined as the frame that clearly demonstrated the first appearance of myocardial blush beyond the IRA (F1). The last frame of TMPFC was then defined as the frame where contrast or myocardial blush disappeared (F2). TMPFC is F2-F1 frame counts at a filming rate of 15 frames/sec, or (F2-F1)×2 frame counts at the corrected filming rate of 30 frames/sec

Secondary

MeasureTime frameDescription
Myocardial-specific isoenzyme of creatine kinase (CK-MB) enzyme levels peri-PCIWithin 0 to 48 hours after enrollmentInfarct size is measured by the myocardial-specific isoenzyme of creatine kinase (CK-MB) area under the curve, calculated by the linear-trapezoidal method. If the baseline or last value is missing, the corresponding value will be set to zero. For missing values of intermediate time points, linear interpolation is used.
TIMI Flow Grade (TFG)One mins after PCITIMI Flow Grade (TFG)assesses flow in the epicardial arteries
TIMI Frame Count (CTFC)One mins after PCICTFC is a continuous measurement assessing flow in the epicardial arteries.
CMR defined MVO3-5 days post-infarctMVO was defined as hypoenhanced area within infracted zone measured by CMR
Infarct Size by Cardiac Magnetic Resonance Imaging (CMR)3-5 days post-infarctInfarct size (expressed as a percentage of LV myocardial mass) between two groups 3-5 days post-infarct assessed by the extent of late gadolinium enhancement on CMR
Wall motion score index (WMSI) and LVEF by echocardiographyEchocardiography was performed 3-5 days after PCIEchocardiographic index includes WMSI and LVEF
ST-segment Resolution90 mins after PCIResolution of the initial sum of ST-segment elevation ≥ 70%

Other

MeasureTime frameDescription
MACEin-hospital (within 14 days)MACE includes all cause death, reinfarction, target vessel revascularization, and stroke

Countries

China

Contacts

Primary ContactBen He, MD,PhD
heben1025@hotmail.com68383609

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026