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Safety and Feasibility of Transcatheter Injectable Hydrogel in Acute STEMI Reperfusion Injury (REFINE Study)

15 maggio 2026 aggiornato da: Myomed Technology (Shaoxing) Co., Ltd.

Clinical Application Study on the Safety and Feasibility of Transcatheter Injectable Protein Alginate-based Hydrogel for Alleviating Reperfusion Injury in Acute STEMI

The purpose of this clinical trial is to preliminarily evaluate the safety and feasibility of the transcatheter injectable protein alginate-based hydrogel developed and manufactured by Myomed Technology (Shaoxing) Co., Ltd. in alleviating reperfusion injury in acute STEMI. This is a randomized controlled trial with a blank control group (conventional PCI treatment). A total of 20 patients will be enrolled in a 1:1 ratio into the test group and the control group.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

20

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • Shaanxi
      • Xi'an, Shaanxi, Cina
        • First Affiliated Hospital of Air Force Medical University
        • Investigatore principale:
          • Fei Li
        • Contatto:
          • Clinical Research Associate
          • Numero di telefono: 021-0575-88605679
          • Email: Welly_wwx@126.com
        • Sub-investigatore:
          • Yali Yang

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  1. Aged 18 to 80 years;
  2. Diagnosed with first-onset acute anterior wall ST-segment elevation myocardial infarction (STEMI), requiring primary percutaneous coronary intervention (PCI) and stent implantation;
  3. 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;
  4. The time interval from the onset of ischemic symptoms to the first PCI balloon dilation is ≤12 hours;
  5. 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;
  6. 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:

  1. 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;
  2. 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;
  3. History of previous myocardial infarction, coronary intervention (PCI), or coronary artery bypass grafting (CABG);
  4. Cerebrovascular accident (CVA) or transient ischemic attack (TIA) within the past 3 months;
  5. Heart failure severity at admission reaches Killip classification Grade III or above;
  6. Complicated with malignant arrhythmia, complete atrioventricular block, or new-onset complete left bundle branch block (LBBB);
  7. Diagnosed or suspected aortic dissection;
  8. Diabetes mellitus with severe complications;
  9. Complicated with atrial fibrillation and receiving only warfarin treatment, or with a high bleeding risk;
  10. Received thrombolytic therapy prior to PCI;
  11. Diameter of the infarct-related artery < 2 mm or abundant coronary collateral circulation in the risk area;
  12. Coronary angiography indicates diffuse vascular lesions or severe calcification that may affect the absorption of protein alginate-based hydrogel;
  13. Severe complications (e.g., coronary artery rupture, perforation, or stent dislodgement) occurring during PCI;
  14. Received coronary bioresorbable stent implantation;
  15. Complicated with severe acute infection requiring systemic treatment;
  16. Currently diagnosed with malignant tumor or receiving malignant tumor treatment;
  17. Severe autoimmune disease requiring therapeutic intervention;
  18. History of severe anemia (hemoglobin < 60 g/L) or thrombocytopenia (platelet count < 100×10⁹/L);
  19. Known renal insufficiency (including estimated creatinine clearance < 30 ml/min/1.73 m², or receiving treatment for severe renal insufficiency);
  20. Alanine aminotransferase (ALT) level exceeding 3 times the upper limit of normal, with the investigator judging clinically significant liver dysfunction;
  21. Known allergy to the study product or any radiocontrast agent;
  22. Contraindications to cardiovascular magnetic resonance (CMR) examination (e.g., implanted cardiac pacemaker, implantable cardioverter-defibrillator, nerve stimulator, cerebral aneurysm clip, cochlear implant, or claustrophobia);
  23. Cognitive dysfunction, dementia, or severe mental illness;
  24. Currently participating in other clinical trials and have not yet reached the primary endpoint;
  25. Expected survival period < 1 year due to comorbidities;
  26. Pregnant or lactating women, or fertile subjects who do not take effective medical contraceptive measures during the study period;
  27. Other factors that the investigator deems may have a significant impact on result judgment or the safety and efficacy of the subjects.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Hydrogel Group
Experimental group: PCI combined with the locally injectable inert material
Altro: Blank Control Group
Conventional PCI procedure

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Incidence of Major Adverse Events (MAEs) within 30 days after surgery
Lasso di tempo: 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)
Lasso di tempo: 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.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Incidence of serious adverse events and device-related adverse events
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 1 day, 3 days and 7days post-procedure
1 day, 3 days and 7days post-procedure
Concentrations of BNP/NT-proBNP and hsCRP
Lasso di tempo: 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.
Lasso di tempo: 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.
Lasso di tempo: 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).
Lasso di tempo: 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
Lasso di tempo: 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).
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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.
Lasso di tempo: 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
Lasso di tempo: 7 days, 3 months and 6 months post-procedure
CMR
7 days, 3 months and 6 months post-procedure
Changes in NYHA classification
Lasso di tempo: 7 days, 30 days, 3 months and 6 months post-procedure
7 days, 30 days, 3 months and 6 months post-procedure
Cardiovascular mortality
Lasso di tempo: 6 months post-procedure
6 months post-procedure
Incidence of recurrent myocardial infarction
Lasso di tempo: 6 months post-procedure
6 months post-procedure
Heart failure readmission rate
Lasso di tempo: 6 months post-procedure
6 months post-procedure
All-cause mortality
Lasso di tempo: 6 months post-procedure
6 months post-procedure

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

30 maggio 2026

Completamento primario (Stimato)

30 ottobre 2026

Completamento dello studio (Stimato)

30 aprile 2027

Date di iscrizione allo studio

Primo inviato

9 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

15 maggio 2026

Primo Inserito (Effettivo)

22 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

22 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

15 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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