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Kidney Transplant; ComplicationsNMP-DBDNCT05031052

Normothermic Machine Perfusion (NMP) Versus Static Cold Storage (SCS) in Human Kidney Transplantation

A study testing End-ischemic normothermic oxygenated machine perfusion and Static cold storage in people with Kidney Transplant; Complications and Kidney Failure, run by Charite University, Berlin, Germany at 4 sites in Germany.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Due to organ shortage in kidney transplantation (KT) several strategies have been implemented in an attempt to increase donor pool utilization, including transplantation of extended criteria donor (ECD) allografts. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
End-ischemic normothermic oxygenated machine perfusion and Static cold storage
Could I receive a placebo?
No, everyone receives an active treatment
How many people
194 participants
Where
4 sitesGermany
Study dates
10 May 2022to 31 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Signed informed consent
  • Patients 18 years or older
  • Patients suffering from end-stage kidney disease / kidney failure
  • Listed for kidney transplantation
  • Receiving ECD-allograft

Who cannot join

  • Recipients of living donor kidney transplants
  • Previous kidney transplantation
  • Combined transplantations (liver-kidney, kidney-pancreas, etc.)
  • Participation in other kidney related trials
  • Exposure to an investigational drug within 30 days prior to inclusion
  • Unwilling or unable to follow the procedures outlined in the protocol
  • Mentally or legally incapacitated

Trial locations and contacts

4 sites in 1 country.

Georg Lurje, M.D. contact

+4930450652339

georg.lurje@charite.de

Deniz Uluk, M.D. contact

+4930450622187

deniz.uluk@charite.de

Germany4 sites, 4 recruiting
  • Charité Universitaetsmedizin Berlin, Campus Mitte | Campus Virchow-Klinikum

    Berlin, 13353

    Georg Lurje, M.D., +4930450652339, georg.lurje@charite.de

    M.D.

    Recruiting
  • Medizinische Hochschule Hannover (MHH), Department of Surgery and Transplantation

    Hanover, 30625

    Florian Vondran, M.D., vondran.florian@mh-hannover.de

    Not yet recruiting
  • University Hospital Heidelberg, Department of Surgery and Transplantation

    Heidelberg, 69120

    Arianeb Mehrabi, M.D., arianeb.mehrabi@med.uni-heidelberg.de

    Not yet recruiting
  • Ludwig-Maximilian's University, Campus Grosshadern, Department of General, Visceral, and Transplant Surgery

    Munich, 81377

    Markus Guba, M.D., markus.guba@med.uni-muenchen.de

    Dionysios Koliogiannis, M.D., dionysios.koliogiannis@med.uni-muenchen.de

    Not yet recruiting

Other trials in Germany

About this study

Official title: Normothermic Machine Perfusion (NMP) Compared to Static Cold Storage (SCS) in Donation After Brain Death (DBD) Kidney Transplantation; a Prospective Multicenter Randomized Controlled Trial (NMP-DBD)

Due to organ shortage in kidney transplantation (KT) several strategies have been implemented in an attempt to increase donor pool utilization, including transplantation of extended criteria donor (ECD) allografts. While the transplantation of ECD organs saves patients from waiting-list dropout, these pre-damaged organs exhibit an increased susceptibility to further injury during organ storage and transplantation. Static cold storage (SCS) involves the transportation of procured donor kidneys on ice and has remained the gold standard for organ preservation for decades. SCS relies on hypothermia to reduce cellular metabolism and oxygen demand while achieving a prolonged preservation time of organs. Upon reperfusion, the reintroduction of oxygen to the ischemic kidney leads to a respiratory burst with massive production of mitochondrial reactive oxygen species and subsequent sterile inflammation of the entire organ. This ischemia-reperfusion injury (IRI) is a central predictor of graft and patient survival. Current clinical preservation strategies are unable to meet the challenges of ECD allograft transplantation and there is a great demand to optimize preservation techniques for such high risk ECD allografts.

Currently, two main paradigms prevail in the clinical approach to kidney allograft machine perfusion (MP) in regard to optimized preservation techniques: while end-ischemic hypothermic (HMP) and hypothermic oxygenated MP (HOPE) may be seen as dynamic alternatives of the traditional organ preservation based on hypothermia-induced deceleration of metabolism could not proof a beneficial effect on delayed graft function or primary graft failure, the impact of normothermic perfusion (NMP) on ECD kidney allografts is still missing. NMP aims at re-equilibration of cellular metabolism by preserving the organ at physiological temperatures whilst ensuring sufficient oxygen and nutrient supply. The present trial was therefore designed to provide first level-II evidence for NMP in human KT after donation after brain death (DBD). In total, 194 human kidney grafts will be randomized to either 4 hours of NMP directly before implantation (intervention group; n = 97) or to SCS (control group; n = 97) prior to transplantation. The primary endpoint will be kidney function after 6 months (6-months eGFR). Secondary endpoints include kidney function after 3 and 12 months, incidence of delayed graft function (DGF), primary non-function (PNF) and surgical complications assessed by the comprehensive complication index (CCI).

Read the detailed description

The first human kidney transplantation (KT) was performed by Murray et al. in 1954 and has evolved as the standard treatment for kidney failure (previously referred to as end-stage renal disease (ESRD). In 2020, approximately 7067 patients were listed for KT in Germany, however only 1342 transplantations could be performed due to organ shortage. The number of patients on the waiting list substantially exceeds the number of donors. Around 390 patients died while waiting for a suitable organ on the waiting list, and another 492 patients dropped out due to morbidity and advancing disease. For increasing donor pool utilization several strategies have been aimed, including living donation, old-for-old KT and transplantation of extended criteria donor (ECD) allografts. While, ECD allografts are associated with a higher incidence of graft related complications and impaired postoperative outcome, novel preservation techniques such as ex-vivo machine perfusion (MP) of the donor allograft have been developed aiming at optimizing the function of marginal organs after transplantation.

The common practice of static cold storage (SCS) organ preservation has changed little since the initial introduction of the original University of Wisconsin (UW) organ preservation solution in the late 1980s. Static organ preservation relies on hypothermia to decelerate metabolism and reduce oxygen demand to prolong ischemia tolerance and avoid rapid functional graft impairment, thereby delaying graft damage. While a significant amount of anaerobic metabolism continues at a low rate, the metabolism of the allograft does not cease completely during SCS. In addition, the lack of blood flow-derived shear stress causes a disruption of endogenous nitric-oxide (NO) production and a functional impairment of endothelial cells. Upon reperfusion, the reintroduction of oxygen-rich blood to the ischemic allograft leads to a respiratory-burst with massive reactive oxygen species (ROS) production, mitochondrial oxidative stress and a sterile inflammatory reaction that is pivotal to kidney injury. This cascade of ischemia-reperfusion injury (IRI) ultimately leads to an impaired outcome, especially in the ECD-KT setting. While high-quality grafts are usually less prone to IRI, ECD allografts exhibit an impaired microcirculation and an increased susceptibility to inflammatory and oxidative stress and, as such, poorly tolerate extended periods of cold storage.

In recent years, MP has been recognized as a promising strategy in the context of ECD kidney transplantation. While SCS only prolongs storage time and limits the damage sustained during the period of cold ischemia, MP can reverse some of these effects.

Hypothermic (HMP) and hypothermic oxygenated MP (HOPE) may be seen as dynamic cold organ preservation based on hypothermia-induced deceleration of metabolism, which aims to combine the positive effects of hypothermia observed in classical cold storage with the positive effects of dynamic preservation. In contrast normothermic perfusion (NMP) mimics physiological circumstances and provides sufficient oxygen and nutrient supply.

End-ischemic HMP with oxygen (HOPE) presents is marked by active oxygenation of the perfusate during MP. Even though beneficials effects of HOPE were reported in preclinical studies, no significant impact on DGF, PNF or graft survival after one year in human KT could be demonstrated. In contrast to hypothermic preservation methods, data on NMP in human KT is limited. In fact, there are no registered randomized controlled clinical trials (RCT), comparing end-ischemic NMP versus SCS in donation after brain death (DBD), the only legal donation circumstance in Germany.

The aim of this study is to investigate the impact of end-ischemic NMP compared to SCS in a multicenter prospective randomized controlled clinical trial (RCT) using ECD kidney allografts from DBD donors.

Being tested
End-ischemic normothermic oxygenated machine perfusion, Static cold storage
Keywords
ex-vivo machine perfusion, normothermic machine perfusion, kidney transplantation, extended criteria donation, donation after brain death, NMP
Medical subject headings
Renal Insufficiency

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • End-ischemic normothermic oxygenated machine perfusionDevice

    Also called NMP

    Application of end-ischemic normothermic oxygenated machine perfusion at physiological temperatures for 4 hours.

  • Static cold storageProcedure or surgery

    Also called SCS

    Immediate implantation of kidney allograft after conventional and static preservation on ice

Study groups in NCT05031052
Study groupRoleWhat they receive
Normothermic machine perfusion (NMP)ExperimentalEnd-ischemic NMP will be performed immediately after arrival of the allocated and static cold stored ECD kidney graft. The study protocol aims a duration of 4 hours. Machine perfusion will be performed with a combination of patient's blood group matched packed red blood cells (RBC) and a special manufactured solution with the currently only certified device in Europe (XVIVO - KidneyAssist®). After 4 hours of perfusion and viability assessment, the kidney allograft will be disconnected from the device immediately prior to transplantation and flushed with three litres of Custodiol HTK solution via the renal artery. Then transplantation will be performed in typical method.
Receives: Device: End-ischemic normothermic oxygenated machine perfusion
Statical cold storage (SCS)Active comparatorConventional method kidney transplantation of statical cold stored and transported ECD kidney allograft. The allocated kidney allograft will be flushed with Custodiol HTK solution during back table preparation with the aim of immediate implantation into recipient.
Receives: Procedure: Static cold storage

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Kidney function

    Estimated glomerular filtration rate (eGFR)

    Measured: After 6 months postoperatively

Secondary outcomes (10)
  1. Kidney function

    Estimated glomerular filtration rates (eGFR)

    Measured: After 3- and 12 months postoperatively

  2. Delayed graft function

    Incidence (absolute and percentage numbers) and duration (in days) of delayed graft function (defined as the period between kidney transplant and last dialysis)

    Measured: First 7 postoperative days

  3. Functional delayed graft function

    Incidence (absolute and relative numbers) and duration (in days) of functional DGF (defined as <10% fall in serum creatinine for 3 consecutive days in the first week post-transplantation)

    Measured: First 7 postoperative days

  4. Creatinine change ratio

    Creatinine change ratio at day 2 (referred to day 1) and Creatinine change ratio at day 5 (referred to pretransplant serum Creatinine)

    Measured: Day 2 and day 5 postoperatively

  5. Primary non function (PNF)

    Incidence of PNF descriped as persisting dialysis dependency after kidney transplantation

    Measured: After 3 months postoperatively

  6. Incidence and severity of postoperative complications

    Assessed by the Clavien-Dindo complication score and the comprehensive complication index (CCI®)

    Measured: 90-days and 1-year postoperatively

  7. Hospitalization

    Duration of hospital stay

    Measured: Follow-up duration of 1-year

  8. Cost analysis

    Total costs of treatment and hospital stay

    Measured: Follow-up duration of 1-year

  9. Recipient- and graft survival

    One-year recipient- and graft survival

    Measured: Follow-up duration of 1-year

  10. Acute rejection incidence

    Biopsy proven acute rejection

    Measured: Follow-up duration of 1-year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Sep 2021
  2. Study start10 May 2022
  3. Primary completion31 Dec 2024 (estimated)
  4. Study completion31 Dec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Multicenter prospective randomized controlled trial
Masking
None (open label)
Enrolment
194 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05031052
Sponsor's protocol ID
EA4/172/21
Acronym
NMP-DBD
Status last verified
Jun 2022
First submitted
23 Aug 2021
Last updated
13 Jun 2022
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Tingle SJ, Thompson ER, Figueiredo RS, Moir JA, Goodfellow M, Talbot D, Wilson CH. Normothermic and hypothermic machine perfusion preservation versus static cold storage for deceased donor kidney transplantation. Cochrane Database Syst Rev. 2024 Jul 9;7(7):CD011671. doi: 10.1002/14651858.CD011671.pub3.

    PubMed 38979743

Questions about this trial

What is this clinical trial studying?

A study testing End-ischemic normothermic oxygenated machine perfusion and Static cold storage in people with Kidney Transplant; Complications and Kidney Failure, run by Charite University, Berlin, Germany at 4 sites in Germany.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 13 Jun 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 4 sites in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Georg Lurje, M.D. (+4930450652339, georg.lurje@charite.de), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Kidney function (time frame: After 6 months postoperatively). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05031052, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Jun 2022.

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