ST Segment Elevation Myocardial Infarction Clinical Trial
Official title:
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.
Verified date | August 2017 |
Source | RenJi Hospital |
Contact | Ben He, MD,PhD |
Phone | 68383609 |
heben1025[@]hotmail.com | |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Not yet recruiting |
Enrollment | 600 |
Est. completion date | June 30, 2019 |
Est. primary completion date | June 30, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility |
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. |
Country | Name | City | State |
---|---|---|---|
China | Ren Ji Hospital Afflited to School of Medicine, Shanghai Jiao Tong University | ShangHai |
Lead Sponsor | Collaborator |
---|---|
RenJi Hospital | Ruijin Hospital, Shanghai 10th People's Hospital, Shanghai 6th People's Hospital, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine |
China,
Chinese Society of Cardiology of Chinese Medical Association; Editorial Board of Chinese Journal of Cardiology. [Guideline of non-ST segment elevation acute coronary syndrome]. Zhonghua Xin Xue Guan Bing Za Zhi. 2012 May;40(5):353-67. Chinese. — View Citation
Ding S, Pu J, Qiao ZQ, Shan P, Song W, Du Y, Shen JY, Jin SX, Sun Y, Shen L, Lim YL, He B. TIMI myocardial perfusion frame count: a new method to assess myocardial perfusion and its predictive value for short-term prognosis. Catheter Cardiovasc Interv. 2010 Apr 1;75(5):722-32. doi: 10.1002/ccd.22298. — View Citation
Gibson CM, Cannon CP, Murphy SA, Ryan KA, Mesley R, Marble SJ, McCabe CH, Van De Werf F, Braunwald E. Relationship of TIMI myocardial perfusion grade to mortality after administration of thrombolytic drugs. Circulation. 2000 Jan 18;101(2):125-30. — View Citation
Gurbel PA, Bliden KP, Butler K, Tantry US, Gesheff T, Wei C, Teng R, Antonino MJ, Patil SB, Karunakaran A, Kereiakes DJ, Parris C, Purdy D, Wilson V, Ledley GS, Storey RF. Randomized double-blind assessment of the ONSET and OFFSET of the antiplatelet effects of ticagrelor versus clopidogrel in patients with stable coronary artery disease: the ONSET/OFFSET study. Circulation. 2009 Dec 22;120(25):2577-85. doi: 10.1161/CIRCULATIONAHA.109.912550. Epub 2009 Nov 18. — View Citation
Kidambi A, Mather AN, Motwani M, Swoboda P, Uddin A, Greenwood JP, Plein S. The effect of microvascular obstruction and intramyocardial hemorrhage on contractile recovery in reperfused myocardial infarction: insights from cardiovascular magnetic resonance. J Cardiovasc Magn Reson. 2013 Jun 27;15:58. doi: 10.1186/1532-429X-15-58. — View Citation
Mehran R, Rao SV, Bhatt DL, Gibson CM, Caixeta A, Eikelboom J, Kaul S, Wiviott SD, Menon V, Nikolsky E, Serebruany V, Valgimigli M, Vranckx P, Taggart D, Sabik JF, Cutlip DE, Krucoff MW, Ohman EM, Steg PG, White H. Standardized bleeding definitions for cardiovascular clinical trials: a consensus report from the Bleeding Academic Research Consortium. Circulation. 2011 Jun 14;123(23):2736-47. doi: 10.1161/CIRCULATIONAHA.110.009449. — View Citation
Pu J, Ding S, Shan P, Qiao Z, Song W, Du Y, Shen J, Jin S, He B. Comparison of epicardial and myocardial perfusions after primary coronary angioplasty for ST-elevation myocardial infarction in patients under and over 75 years of age. Aging Clin Exp Res. 2010 Aug;22(4):295-302. doi: 10.3275/6711. Epub 2009 Dec 1. — View Citation
Pu J, Shan P, Ding S, Qiao Z, Jiang L, Song W, Du Y, Shen J, Shen L, Jin S, He B. Gender differences in epicardial and tissue-level reperfusion in patients undergoing primary angioplasty for acute myocardial infarction. Atherosclerosis. 2011 Mar;215(1):203-8. doi: 10.1016/j.atherosclerosis.2010.11.019. Epub 2010 Nov 26. — View Citation
Roe MT, Ohman EM, Maas AC, Christenson RH, Mahaffey KW, Granger CB, Harrington RA, Califf RM, Krucoff MW. Shifting the open-artery hypothesis downstream: the quest for optimal reperfusion. J Am Coll Cardiol. 2001 Jan;37(1):9-18. Review. — View Citation
Shen LH, Wan F, Shen L, Ding S, Gong XR, Qiao ZQ, Du YP, Song W, Shen JY, Jin SX, Pu J, Yao TB, Jiang LS, Li WZ, Zhou GW, Liu SW, Han YL, He B. Pharmacoinvasive therapy for ST elevation myocardial infarction in China: a pilot study. J Thromb Thrombolysis. 2012 Jan;33(1):101-8. doi: 10.1007/s11239-011-0657-7. — View Citation
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* Note: There are 11 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | MACE | MACE includes all cause death, reinfarction, target vessel revascularization, and stroke | in-hospital (within 14 days) | |
Other | MACE | MACE includes all cause death, reinfarction, target vessel revascularization, and stroke | 30 days after randomization | |
Primary | TIMI Myocardial Perfusion Frame Count (TMPFC) | TMPFC 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 | One mins after PCI | |
Primary | TIMI Myocardial Perfusion Frame Count (TMPFC) | TMPFC 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 | One mins after intracoronary medicine infusion post-PCI | |
Primary | TIMI Myocardial Perfusion Grade (TMPG) | TMPG is an angiographic measure of myocardial perfusion | One mins after PCI | |
Primary | TIMI Myocardial Perfusion Grade (TMPG) | TMPG is an angiographic measure of myocardial perfusion | One mins after intracoronary medicine infusion post-PCI | |
Secondary | ST-segment Resolution | Resolution of the initial sum of ST-segment elevation = 70% | 90 mins after PCI | |
Secondary | Myocardial-specific isoenzyme of creatine kinase (CK-MB) enzyme levels peri-PCI | Infarct 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. | Within 0 to 48 hours after enrollment | |
Secondary | TIMI Flow Grade (TFG) | TIMI Flow Grade (TFG)assesses flow in the epicardial arteries | One mins after PCI | |
Secondary | TIMI Flow Grade (TFG) | TIMI Flow Grade (TFG)assesses flow in the epicardial arteries | One mins after intracoronary medicine infusion post-PCI | |
Secondary | TIMI Frame Count (CTFC) | CTFC is a continuous measurement assessing flow in the epicardial arteries. | One mins after PCI | |
Secondary | TIMI Frame Count (CTFC) | CTFC is a continuous measurement assessing flow in the epicardial arteries. | One mins after intracoronary medicine infusion post-PCI | |
Secondary | Wall motion score index (WMSI) and LVEF by echocardiography | Echocardiographic index includes WMSI and LVEF | Echocardiography was performed 3-5 days after PCI | |
Secondary | CMR defined MVO | MVO was defined as hypoenhanced area within infracted zone measured by CMR | 3-5 days post-infarct | |
Secondary | Infarct Size by Cardiac Magnetic Resonance Imaging (CMR) | Infarct 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 | 3-5 days post-infarct |
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