DCB Under the Guidance of OCT in STEMI

Sponsor
Henan Institute of Cardiovascular Epidemiology (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05680051
Collaborator
(none)
300
2
13.9

Study Details

Study Description

Brief Summary

Acute ST segment elevation myocardial infarction (STEMI) has a high disability mortality rate, and timely reperfusion treatment can significantly reduce the mortality of patients. Emergency PCI is the preferred strategy for STEMI treatment recommended by domestic and international guidelines. The long-term existence of stents can never completely avoid the formation of thrombosis in the stents and affect the relaxation and contraction of criminal blood vessels. Drug coated balloon provides a new concept and technology of interventional therapy for coronary artery disease in the form of "intervention without implantation". Through balloon dilation of local blood vessels to release anti proliferative drugs to coronary artery wall and inhibit intimal hyperplasia, it can not only treat serious coronary artery disease, improve coronary blood supply and vascular function, but also not leave permanent implants in the blood vessels; The main pathogenesis of STEMI is thrombosis based on the rupture or erosion of coronary atheromatous plaque. In terms of pathophysiological mechanism, drug coated balloons are also suitable for STEMI patients without obvious thrombosis or severe dissection after full pretreatment. The two-dimensional lumen images obtained by traditional coronary angiography can not directly reflect the vessel wall, so we can not evaluate the actual size of the vessel, plaque characteristics and the effect of intervention through coronary angiography; Optical coherence tomography (OCT) uses near-infrared scanning to produce high-resolution tissue microscopic images with a resolution of up to 10 μ m. It can clearly observe the three-layer structure of coronary artery, find abnormal intima structure, and more clearly identify thrombosis, dissection, plaque erosion or collapse in coronary artery, providing more valuable information for optimizing interventional treatment. Therefore, the application of drug coated balloon under the guidance of OCT in STEMI can provide a more accurate and optimized diagnosis and treatment scheme for STEMI patients.

Condition or Disease Intervention/Treatment Phase
  • Device: Drug-eluting balloon
  • Device: Drug-eluting stent
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Prospective, Multi-center, Randomized, Parallel Controlled Clinical Trial of Drug Coated Balloon Under the Guidance of OCT in the Treatment of Acute ST-segment Elevation Myocardial Infarction
Anticipated Study Start Date :
Dec 31, 2022
Anticipated Primary Completion Date :
Dec 30, 2023
Anticipated Study Completion Date :
Feb 28, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental group

Drug-coated Balloon (Lepu Medical Technology (Beijing) Co.,Ltd.)

Device: Drug-eluting balloon
Drug eluting balloon was used in the experimental group

Active Comparator: Control group

Drug Eluting Stent(Microport Medical)

Device: Drug-eluting stent
Drug eluting stent was used in the control group

Outcome Measures

Primary Outcome Measures

  1. Late lumen loss rate [10 months after discharge.]

Secondary Outcome Measures

  1. Revascularization rate of target lesions [10 months after discharge.]

  2. Target vessel revascularization rate [1 month after discharge, 3 months after discharge, 6 months after discharge, 10 months after discharge.]

  3. Major Adverse Cardiovascular Events [1 month after discharge, 3 months after discharge, 6 months after discharge, 10 months after discharge.]

  4. Cardiovascular death [1 month after discharge, 3 months after discharge, 6 months after discharge, 10 months after discharge.]

  5. Recurrent acute myocardial infarction [1 month after discharge, 3 months after discharge, 6 months after discharge, 10 months after discharge.]

    Time-to-onset for recurrent acute myocardial infarction, as ascertained according to follow-up

  6. Stroke [1 month after discharge, 3 months after discharge, 6 months after discharge, 10 months after discharge.]

    Time-to-onset for stroke, as ascertained according to follow-up

  7. All cause of death [1 month after discharge, 3 months after discharge, 6 months after discharge, 10 months after discharge.]

  8. Unstable angina [1 month after discharge, 3 months after discharge, 6 months after discharge, 10 months after discharge.]

    Time-to-onset for unstable angina, as ascertained according to follow-up

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age 18-75

  2. Definitely diagnosed as acute ST segment elevation myocardial infarction according to diagnostic criteria

  3. Time of onset ≤ 12h

  4. Voluntary signing of informed consent

  5. After pretreatment, the culprit vessel participates in stenosis ≤ 30%, no type C (or OCT shows that the dissection involves the middle membrane, and the angle is ≥ 90 degrees) or above, no hematoma, and no obvious thrombus (TIMI thrombus load rating ≤

Exclusion Criteria:
  1. Time of onset>12h

  2. Those who are allergic to contrast agents, aspirin tablets and Tigrilol tablets;

  3. Active bleeding or recent bleeding history

  4. Cardiogenic shock and long-term cardiopulmonary resuscitation;

  5. The life span is expected to be less than 12 months

  6. Angiography showed left main trunk lesion;

  7. Angiography shows patients with in stent restenosis

  8. Patients who the investigator thinks may affect the normal progress of the study or cannot cooperate well with the study or may cause obvious risks, such as alcoholics or drug abusers, cancer, serious liver, kidney, lung, endocrine (such as uncontrolled diabetes or thyroid disease), nervous or blood system diseases;

  9. Known or suspected pregnancy (baseline ß - hCG pregnancy test must be conducted for women in childbearing period), women in menstrual period.

  10. The criminal blood vessel has C-type or above dissection after pretreatment, and there is coronary hematoma.

  11. After pretreatment, criminal vessels still have obvious thrombus residues (TIMI thrombus load grade ≥ 3)

  12. OCT confirms that the criminal lesion is caused by plaque erosion

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Henan Institute of Cardiovascular Epidemiology

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Henan Institute of Cardiovascular Epidemiology
ClinicalTrials.gov Identifier:
NCT05680051
Other Study ID Numbers:
  • HenanICE202208
First Posted:
Jan 11, 2023
Last Update Posted:
Jan 11, 2023
Last Verified:
Dec 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 11, 2023