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Clinical Trials/NL-OMON29265
NL-OMON29265Not yet recruitingNot Applicable

Arterial Reperfusion or Portal Reperfusion First in Liver Transplantation usingDonation after Circulatory Death donors

Erasmus MC Rotterdam0 sites150 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
150

Study Overview

Brief Summary

  1. Jay C, Ladner D, Wang E, Lyuksemburg V, Kang R, Chang Y, et al. A comprehensive risk assessment of mortality following donation after cardiac death liver transplant - An analysis of the national registry. J Hepatol. 2011 Oct;55(4):808-13. 2. Jay CL, Lyuksemburg V, Kang R, Preczewski L, Stroupe K, Holl JL, et al. The increased costs of donation after cardiac death liver transplantation: caveat emptor. Ann Surg. 2011 Apr;251(4):743-8. 3. Jay CL, Lyuksemburg V, Ladner DP, Wang E, Caicedo JC, Holl JL, et al. Ischemic cholangiopathy after controlled donation after cardiac death liver transplantation: a meta-analysis. Ann Surg. 2011 Feb;253(2):259-64. 4. Farid WR, de Jonge J, Slieker JC, Zondervan PE, Thomeer MG, Metselaar HJ, et al. The importance of portal venous blood flow in ischemic-type biliary lesions after liver transplantation. Am J Transplant. 2011 Apr;11(4):857-62.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • Age over 18 years of age
  • - On the active waiting list for liver transplantation
  • - Foreseen to be offered a donation after circulatory death (DCD) liver graft
  • - Written informed consent for this trial

Exclusion Criteria

  • - Contra-indications for DCD liver graft
  • - Split or reduced liver grafts
  • - Technical contra-indications to arterial reperfusion within 45 minutes (need for vascular reconstructions, jump grafting etc. during warm ischemic period)
  • - Multi-organ transplantation
  • - Pregnancy

Investigators

Sponsor
Erasmus MC Rotterdam

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