Ask to take part

Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Mr Dorian Verscheure
+33 (0)63291212
dorians@gmail.com


Study Location:

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Be Part of Research - Trial Details - Endovascular treatment of aortic arch chronic dissection with a branched endograft following previous ascending aorta replacement for Acute Type A dissection: midterm results from an international multicenter study

Endovascular treatment of aortic arch chronic dissection with a branched endograft following previous ascending aorta replacement for Acute Type A dissection: midterm results from an international multicenter study

Medical Conditions

Aortic arch chronic dissection following ascending aorta prosthetic replacement for acute Stanford A dissection


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


Acute aortic dissection is a disease with a risk of rupture of the ascending aorta (the part of the aorta after the heart) that can be treated with prosthetic replacement of the ascending aorta. After the repair and during follow up of those patients, the residual part of the aorta (the aortic arch) can heal with time. In other cases, the remaining persistent dissected part of the aorta can grow in diameter leading to an aneurysm (bulge). In this case, there is a risk of rupture of the aneurysm causing the death of the patient. The only way to prevent this rupture is a preventive surgery of the dilated part of the aorta. The conventional treatment for those aneurysms is a surgical replacement of the aortic arch. This surgery has high mortality and morbidity rates. This surgery is performed under general anaesthesia and requires extracorporeal circulation (circulation of blood outside the body through a machine) with hypothermic circulatory arrest (temporarily stopping blood flow under very cold body temperatures). Only healthy patients can undergo this surgery. Recently, a group of surgeons have used an endovascular approach for degenerative aneurysm of the aortic arch (non dissecting aneurysms). The device used is a long covered stent (tube) with two branches to keep supra aortic vessels (for the brain and the arms) patent (open). This device is custom made for each patient's anatomy. This technique had acceptable mortality and morbidity rates. The encouraging results of the early experience with this device have led to the use of this technique in chronic dissection of the aortic arch. The aim of this study is to assess the results of this endovascular treatment of dissecting aneurysm of the aortic arch in patients previously treated for an acute aortic dissection.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

02 Dec 2017 01 Apr 2018

Publications

2021 Results article in https://www.ncbi.nlm.nih.gov/pubmed/30973389/ results

Data about patients treated with this device around the world are collected and analysed. Rates of in-hospital mortality and stroke, technical success, early and late complications, re-intervention, and mortality during follow-up are evaluated.


Patients aged 18 or older previously treated for an acute aortic dissection with a custom-made branched endograft

You can take part if:



You may not be able to take part if:


Does not meet inclusion criteria


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • St Thomas' Hospital
    London
    SE1 7EH
  • Centre Chirurgical Marie Lannelongue
    133 avenue de la résistance
    Le Plessis-Robinson
    92350
  • University Hospital Eppendorf
    20246
  • CHU de Lille
    59000
  • Skane University Hospital
    214 28
  • Uppsala University Hospital
    751 85
  • Cleveland Clinic
    44195
  • Serviço Integrado de Técnicas Endovasculares
    22031-070
  • Maastricht University Medical Center
    6202 AZ
  • University Medical Center Regensburg
    93053
  • Queen Elizabeth University Hospital NHS Foundation Trust
    B15 2TH
  • CHU de Nantes
    44093
  • Medical University of Warsaw
    02-091

There are no benefits and risks for participating patients in this study. Patients would have the same surgical repair with or without recruitment into this study. The benefits of this endovascular repair are low mortality and stroke rates in the short term. The risk of this endovascular approach is a high late re-intervention rate.

Mr Dorian Verscheure
+33 (0)63291212
dorians@gmail.com



The study is sponsored by Centre Chirurgical Marie Lannelongue and funded by Investigator initiated and funded.




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Read full details for Trial ID: ISRCTN16716994
Last updated 23 April 2019

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