Status:

UNKNOWN

Guo's Entry Tear Repair :The First in Man Study of Endopatch System

Lead Sponsor:

Hangzhou Endonom Medtech Co., Ltd.

Conditions:

Chronic Stanford B Type Aortic Dissection Proximal Tear

Eligibility:

All Genders

18-80 years

Phase:

NA

Brief Summary

A prospective, single-center, first in man study to evaluate the safety and efficacy of Endopatch System manufactured by Hangzhou Endonom Medtech Co., Ltd. for the Chronic Stanford B type aortic disse...

Eligibility Criteria

Inclusion

  • Patients aged 18 to 80 years old, no gender limitation;
  • Able to understand the purpose of the trial, participate in the trial voluntarily with informed consent form signed by the patient him/herself or his or her legal representative, and willing to complete follow-up visits as required under the protocol;
  • Diagnosed as chronic Stanford type B aortic dissection;
  • Maximum diameter of the intimal tears is between 2mm and 20mm;
  • Important branch vessels will not be covered after intimal tears closure;
  • Aortic endovascular treatment can be performed with appropriate arterial access.

Exclusion

  • Diagnosed as acute, subacute aortic dissection;
  • Intermural hematoma, aortic ulcer, pseudoaneurysm, and severe aortic calcification;
  • The minimum distance between the intimal tears of the aortic intimal flaps and the root of the intimal flaps is less than the radius of the patch to be used (the patch cannot be deployed flat);
  • Pregnant, breastfeeding or cannot contraception during the trial period;
  • Participated in clinical trials of other drugs or devices during the same period;
  • The same operation requires intervention in other vascular diseases (such as coronary artery, renal artery, superior mesenteric artery, etc.), and the postoperative drug treatment plan is therefore affected;
  • Allergic to contrast agents, anesthetics, patches, and delivery materials;
  • Cannot tolerate anesthesia;
  • Severe liver, kidney, lung, and heart function abnormalities before surgery \[Serum creatinine exceeds 2 times the upper limit of normal; Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) exceeds 5 times the upper limit of normal; Serum total bilirubin (STB) more than 2 times the upper limit of normal; Left ventricular ejection fraction is lower than normal by cardiac color Doppler ultrasound examination\];
  • History of myocardial infarction, TIA or cerebral infarction within the past 3 months;
  • Life expectancy is less than 12 months (such as advanced malignant tumors)
  • Acute systemic infection
  • Investigator judged that not suitable for interventional treatment.

Key Trial Info

Start Date :

April 15 2021

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 15 2023

Estimated Enrollment :

27 Patients enrolled

Trial Details

Trial ID

NCT04745039

Start Date

April 15 2021

End Date

December 15 2023

Last Update

July 19 2023

Active Locations (1)

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1

Chinese PLA General Hospital

Beijing, China