Safety and Feasibility of Transcatheter Injectable Hydrogel in Acute STEMI Reperfusion Injury (REFINE Study)
Clinical Application Study on the Safety and Feasibility of Transcatheter Injectable Protein Alginate-based Hydrogel for Alleviating Reperfusion Injury in Acute STEMI
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Contact
Study Contact
- Name: Clinical Medical Director
- Phone Number: 86-17621666472
- Email: contact@myomedtech.com
Study Locations
-
-
Shaanxi
-
Xi'an, Shaanxi, China
- First Affiliated Hospital of Air Force Medical University
-
Principal Investigator:
- Fei Li
-
Contact:
- Clinical Research Associate
- Phone Number: 021-0575-88605679
- Email: Welly_wwx@126.com
-
Sub-Investigator:
- Yali Yang
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged 18 to 80 years;
- Diagnosed with first-onset acute anterior wall ST-segment elevation myocardial infarction (STEMI), requiring primary percutaneous coronary intervention (PCI) and stent implantation;
- Ischemic symptoms (e.g., chest pain, precordial discomfort) persist for >30 minutes, and electrocardiographic findings meet the following criteria: ST-segment (J-point) elevation ≥1.0 mm (i.e., amplitude 0.1 mV) in all conventional leads except leads V2 and V3. For leads V2 and V3, the ST-segment elevation criteria are: ≥2.5 mm in males <40 years old, ≥2.0 mm in males ≥40 years old, and ≥1.5 mm in females of all ages;
- The time interval from the onset of ischemic symptoms to the first PCI balloon dilation is ≤12 hours;
- Admission coronary angiography shows that the left anterior descending artery (LAD) has a TIMI flow grade of 0 (complete occlusion), and the TIMI flow grade reaches 3 after stent implantation;
- Able to understand the purpose of the trial, voluntarily participate in the study, sign the informed consent form personally or via a legal representative, and be willing to complete the follow-up in accordance with the protocol requirements.
Exclusion Criteria:
- Complicated with cardiogenic shock or cardiac arrest; or complicated with acute myocardial infarction mechanical complications requiring surgical or interventional intervention (e.g., ventricular septal perforation, papillary muscle rupture, free wall rupture), or complicated with giant left ventricular aneurysm;
- Previously diagnosed with hypertrophic cardiomyopathy, hemodynamically significant congenital heart disease, severe valvular heart disease, chronic cor pulmonale, chronic heart failure, or with a history of cardiac tamponade, pericarditis, or myocarditis;
- History of previous myocardial infarction, coronary intervention (PCI), or coronary artery bypass grafting (CABG);
- Cerebrovascular accident (CVA) or transient ischemic attack (TIA) within the past 3 months;
- Heart failure severity at admission reaches Killip classification Grade III or above;
- Complicated with malignant arrhythmia, complete atrioventricular block, or new-onset complete left bundle branch block (LBBB);
- Diagnosed or suspected aortic dissection;
- Diabetes mellitus with severe complications;
- Complicated with atrial fibrillation and receiving only warfarin treatment, or with a high bleeding risk;
- Received thrombolytic therapy prior to PCI;
- Diameter of the infarct-related artery < 2 mm or abundant coronary collateral circulation in the risk area;
- Coronary angiography indicates diffuse vascular lesions or severe calcification that may affect the absorption of protein alginate-based hydrogel;
- Severe complications (e.g., coronary artery rupture, perforation, or stent dislodgement) occurring during PCI;
- Received coronary bioresorbable stent implantation;
- Complicated with severe acute infection requiring systemic treatment;
- Currently diagnosed with malignant tumor or receiving malignant tumor treatment;
- Severe autoimmune disease requiring therapeutic intervention;
- History of severe anemia (hemoglobin < 60 g/L) or thrombocytopenia (platelet count < 100×10⁹/L);
- Known renal insufficiency (including estimated creatinine clearance < 30 ml/min/1.73 m², or receiving treatment for severe renal insufficiency);
- Alanine aminotransferase (ALT) level exceeding 3 times the upper limit of normal, with the investigator judging clinically significant liver dysfunction;
- Known allergy to the study product or any radiocontrast agent;
- Contraindications to cardiovascular magnetic resonance (CMR) examination (e.g., implanted cardiac pacemaker, implantable cardioverter-defibrillator, nerve stimulator, cerebral aneurysm clip, cochlear implant, or claustrophobia);
- Cognitive dysfunction, dementia, or severe mental illness;
- Currently participating in other clinical trials and have not yet reached the primary endpoint;
- Expected survival period < 1 year due to comorbidities;
- Pregnant or lactating women, or fertile subjects who do not take effective medical contraceptive measures during the study period;
- Other factors that the investigator deems may have a significant impact on result judgment or the safety and efficacy of the subjects.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Hydrogel Group
|
Experimental group: PCI combined with the locally injectable inert material
|
|
Other: Blank Control Group
|
Conventional PCI procedure
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Incidence of Major Adverse Events (MAEs) within 30 days after surgery
Time Frame: within 30 days
|
Defined as all-cause death, stroke, target vessel myocardial infarction, new-onset severe heart failure, cardiac arrest, cardiogenic shock, sustained ventricular arrhythmia, target vessel revascularization, and any device-related complications.
|
within 30 days
|
|
Myocardial Salvage Index (MSI)
Time Frame: 7 days, 3 months and 6 months post-procedure.
|
Score range: 0 to 1.0.
Higher MSI values indicate better myocardial salvage and superior clinical outcome; lower values indicate smaller salvaged myocardial area and worse outcome.
|
7 days, 3 months and 6 months post-procedure.
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Incidence of serious adverse events and device-related adverse events
Time Frame: 7 days, 30 days, 3 months, and 6 months post-procedure
|
7 days, 30 days, 3 months, and 6 months post-procedure
|
|
|
Immediate surgical success
Time Frame: Immediately after the procedure
|
Defined as successful delivery of the investigational product to the predefined target site via catheter, satisfactory immediate angiographic results, uneventful catheter withdrawal, and absence of serious adverse events throughout the procedure.
|
Immediately after the procedure
|
|
AUC of CK-MB and hs-cTnI
Time Frame: baseline, 1 day, 3 days and 7 days post-procedure
|
baseline, 1 day, 3 days and 7 days post-procedure
|
|
|
Changes in interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) levels
Time Frame: 1 day, 3 days and 7days post-procedure
|
1 day, 3 days and 7days post-procedure
|
|
|
Concentrations of BNP/NT-proBNP and hsCRP
Time Frame: baseline, 1 day, 3 days, 7days and 6 months post-procedure
|
baseline, 1 day, 3 days, 7days and 6 months post-procedure
|
|
|
To assess changes in the grade of Segmental Wall Motion Abnormality (SWMA) in target segments based on the ASE 17-segment model, as well as the reduction rate of segments with wall motion abnormalities.
Time Frame: 7 days, 3 months and 6 months post-procedure
|
CMR and TTE
|
7 days, 3 months and 6 months post-procedure
|
|
To evaluate changes in mean Segmental Wall Thickening Rate (SWTR) of target segments.
Time Frame: 7 days, 3 months and 6 months post-procedure
|
CMR
|
7 days, 3 months and 6 months post-procedure
|
|
To evaluate changes in left ventricular global longitudinal strain (LVGLS).
Time Frame: 7 days, 3 months and 6 months post-procedure
|
CMR and TTE
|
7 days, 3 months and 6 months post-procedure
|
|
To evaluate changes in myocardial perfusion status
Time Frame: 7 days, 3 months and 6 months post-procedure
|
CMR first pass perfusion imaging (PFI)
|
7 days, 3 months and 6 months post-procedure
|
|
To evaluate changes in myocardial extracellular volume (ECV).
Time Frame: 7 days, 3 months and 6 months post-procedure
|
CMR
|
7 days, 3 months and 6 months post-procedure
|
|
To evaluate change in left ventricular end-diastolic volume (LVEDV)
Time Frame: 7 days, 3 months and 6 months post-procedure
|
Detection method: cardiac magnetic resonance (CMR) and transthoracic echocardiography (TTE)
|
7 days, 3 months and 6 months post-procedure
|
|
To evaluate change in left ventricular end-systolic volume (LVESV)
Time Frame: 7 days, 3 months and 6 months post-procedure
|
Detection method: cardiac magnetic resonance (CMR) and transthoracic echocardiography (TTE)
|
7 days, 3 months and 6 months post-procedure
|
|
To evaluate change in left ventricular ejection fraction (LVEF)
Time Frame: 7 days, 3 months and 6 months post-procedure
|
Detection method: cardiac magnetic resonance (CMR) and transthoracic echocardiography (TTE)
|
7 days, 3 months and 6 months post-procedure
|
|
To evaluate changes in Transmural Myocardial Infarction (TMI) grade
Time Frame: 7 days, 3 months and 6 months post-procedure
|
CMR
|
7 days, 3 months and 6 months post-procedure
|
|
To evaluate changes in intramyocardial hemorrhage (IMH) area.
Time Frame: 7 days, 3 months and 6 months post-procedure
|
CMR
|
7 days, 3 months and 6 months post-procedure
|
|
To evaluate changes in myocardial infarct size
Time Frame: 7 days, 3 months and 6 months post-procedure
|
CMR
|
7 days, 3 months and 6 months post-procedure
|
|
Changes in NYHA classification
Time Frame: 7 days, 30 days, 3 months and 6 months post-procedure
|
7 days, 30 days, 3 months and 6 months post-procedure
|
|
|
Cardiovascular mortality
Time Frame: 6 months post-procedure
|
6 months post-procedure
|
|
|
Incidence of recurrent myocardial infarction
Time Frame: 6 months post-procedure
|
6 months post-procedure
|
|
|
Heart failure readmission rate
Time Frame: 6 months post-procedure
|
6 months post-procedure
|
|
|
All-cause mortality
Time Frame: 6 months post-procedure
|
6 months post-procedure
|
Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- MR-002-CARP-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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