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

15. mai 2026 oppdatert av: 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.

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

20

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Shaanxi
      • Xi'an, Shaanxi, Kina
        • First Affiliated Hospital of Air Force Medical University
        • Hovedetterforsker:
          • Fei Li
        • Ta kontakt med:
          • Clinical Research Associate
          • Telefonnummer: 021-0575-88605679
          • E-post: Welly_wwx@126.com
        • Underetterforsker:
          • Yali Yang

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

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.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Hydrogel Group
Experimental group: PCI combined with the locally injectable inert material
Annen: Blank Control Group
Conventional PCI procedure

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Incidence of Major Adverse Events (MAEs) within 30 days after surgery
Tidsramme: 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)
Tidsramme: 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.

Sekundære resultatmål

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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

30. mai 2026

Primær fullføring (Antatt)

30. oktober 2026

Studiet fullført (Antatt)

30. april 2027

Datoer for studieregistrering

Først innsendt

9. mai 2026

Først innsendt som oppfylte QC-kriteriene

15. mai 2026

Først lagt ut (Faktiske)

22. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

22. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

15. mai 2026

Sist bekreftet

1. mai 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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