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Therapeutic Hypothermia in "Expanded Criteria" Brain-dead Donors and Kidney-graft Function (HYPOREME)

Primary Purpose

Organ Donor, Brain Death, Kidney Transplant; Complications

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Procedure control: normothermia
Procedure active
Sponsored by
Nantes University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Organ Donor

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • For donors: legal determination of death by neurologic criteria/deceased organ donor/no medical contre-indication to donation/Information given to the authorizing surrogate/ Pregnant women.

    • For transplant recipients : age 18 years or greater /information given and no opposition signed by recipients.

Exclusion Criteria:

  • For donors: no legal determination of death by neurologic criteria/not a deceased organ donor/ medical contre-indication to donation/ no Information given to the authorizing surrogate.
  • For transplant recipients: age <18 years / no information given and/or opposition signed by recipients.

Sites / Locations

  • CHU Amiens-Picardie
  • CHU d'Angers
  • CH Angouleme
  • CH Avignon
  • CH de Blois
  • CHU de Bordeaux
  • CH Bourges
  • CHU Brest
  • CHU Caen
  • Ch Cholet
  • Chu Clermont Ferrand
  • Hopital Henri Mondor
  • CHU de Dijon
  • CH de Dreux
  • CHU Grenoble
  • CH Marne la Vallée (GHEF)
  • CH La Roche sur Yon
  • CH La Rochelle
  • CH Laval
  • Hopital Bicetre
  • CH Le Mans
  • CHRU Lille
  • CHU Limoges
  • CH Lorient
  • CHU de Lyon
  • Hopital de la Conception
  • Hopital de la Timone
  • CH de Meaux (GHEF)
  • CHU Montpellier
  • CH Morlaix
  • Nantes University Hospital
  • CHU Nice
  • CH Orléans
  • Hopital Saint Louis
  • Hopital de la Pitié Salpetriere
  • Hopital Necker
  • CHU Tenon
  • CHU Poitiers
  • CH Annecy Genevois
  • CH Cornouaille
  • CHU Reims
  • CHU Rennes
  • CHU Rouen
  • CH Saint Brieuc
  • CH Saint Nazaire
  • CH Saint Malo
  • CHRU Saint-Etienne
  • CH Saintes
  • CHU Strasbourg
  • CHU Foch
  • CHU Toulouse
  • CHU Tours
  • CHRU Nancy
  • CH Vannes

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Experimental

Arm Label

NT normothermia

HT mild hypothermia

Arm Description

After information for donation and research has been explained, organ donors in the normothermia (NT) group will either be maintained to spontaneously reach a body temperature of 36,5 °C-37,5°, until transfer to the operating room.

The intervention will take place after information for donation and research has been explained . Organ donors in the intervention group will either be actively warmed or allowed to reach a body temperature of 34 °C-35°C, until transfer to the operating room.

Outcomes

Primary Outcome Measures

rate of patients with delayed graft function (DGF)
DGF is the recipient's requirement for dialysis during the first week after transplantation. To show the interest of Targeted Temperature Management in order to optimize the functional recovery of transplanted kidney transplants by comparing 2 groups of recipient subjects: those receiving one Graft from an "expanded criteria donors" maintained in hypothermia (34°-35°) and those receiving a graft from an "expanded criteria donors" maintained in normothermia (36,5°-37,5°).

Secondary Outcome Measures

Temperature Profile
comparison of temperature profile between the two arms
Severe arrhythmias
Severe arrythmia will be define by salvo of ventricular extrasystole, ventricular fibrillation, ventricular tachycardia, need an external shock, need anti-arrhythmic treatment. Participants will be followed for the duration of Intensive Care Unit stay and/or operating room, an expected average of 24 hours.
Cardiac arrest
SParticipants will be followed for the duration of Intensive Care Unit stay and/or operating room, an expected average of 24 hours.
Occurrence of hypotension measured by Total dose of inotropic drugs
Total dose of different inotropic drugs (Epinephrine, Norepinephrine, Dobutamine) will be compare between 2 groups during targetted controlled temperature management period.
Occurrence of hypotension measured by cumulative fluid balance
Cumulative fluid balance will be compare between 2 groups during targetted controlled temperature management period
occurrence of cardiac arrest
comparison of occurrence of cardiac arrest between the two arms
Kidney function measured by serum creatinine value
Kidney function measured by serum creatinine value
Kidney function measured by CKD EPI score
Kidney function measured by CKD EPI score (= 141 x min(Scr/K,1)a x max(Scr/K,1)-1,209 x 0,993Age x 1,018 (for women))
electrolyte balance : potassium, calcium, sodium concentration disorders in mmoL/L
Potential hypothermia related side effects
glycemia in mmoL/L
Potential hypothermia related side effects
liver disorder (ASAT, ALAT, GGT, PAL , BILI in UI/L )
Potential hypothermia related side effects
thrombocytopenia in mm3/L
Potential hypothermia related side effects
Number of individual organs transplanted
Participants will be followed for the duration of Intensive care unit length of stay, and operating room, an average of 24 hours.
Hospital mortality
Participants will be followed for the duration of hospital stay, an expected average of 1 week.
Kidney function measured by serum creatinine value
Kidney function measured by serum creatinine value at day7
Kidney function measured by CKD EPI
Kidney function measured by CKD EPI (= 141 x min(Scr/K,1)a x max(Scr/K,1)-1,209 x 0,993Age x 1,018 (for women))
Extra renal support requirement
Extra renal support requirement at Day7
Kidney graft acute rejection
Kidney graft acute rejection
Acute pulmonary oedema by left ventricular failure
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days.
Severe arrythmia
Severe arrythmia will be define by salvo of ventricular extrasystole, ventricular fibrillation, ventricular tachycardia, need an external shock, need anti-arrhythmic treatment. Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Pulmonary embolism
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Acute coronary syndrome
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Nosocomial Bloodstream infection
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Early onset pneumonia
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Central Venous Catheter infection
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Urinary tract sepsis
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Mortality at D28
comparison of mortality at D28 between the two arms
Mortality at 3 months
comparison of mortality at 3months between the two arms
Mortality at 1 year
comparison of mortality at 1 year between the two arms
Length of hospital stay
comparison of length of hospital stay between the two arms
Kidney function measured by serum creatinine value
Kidney function measured by serum creatinine value
Kidney function measured by CKD EPI
Kidney function measured by CKD EPI (= 141 x min(Scr/K,1)a x max(Scr/K,1)-1,209 x 0,993Age x 1,018 (for women)) at Day28
Extra renal support requirement defined by percentage of patients requiring at least one dialysis
Extra renal support requirement
Kidney graft acute rejection
Kidney graft acute rejection
Acute pulmonary oedema by left ventricular failure
Acute pulmonary oedema by left ventricular failure
Severe arrythmia
Severe arrythmia will be define by salvo of ventricular extrasystole, ventricular fibrillation, ventricular tachycardia, need an external shock, need anti-arrhythmic treatment.
Pulmonary embolism
Pulmonary embolism
Acute coronary syndrome
Acute coronary syndrome
Nosocomial Bloodstream infection
Nosocomial Bloodstream infection
Early onset pneumonia
Early onset pneumonia
Central Venous Catheter infection
Central Venous Catheter infection
Urinary tract sepsis
Urinary tract sepsis
Kidney function measured by serum creatinine value
Kidney function measured by serum creatinine value
Kidney function measured by CKD EPI
Kidney function measured by CKD EPI (= 141 x min(Scr/K,1)a x max(Scr/K,1)-1,209 x 0,993Age x 1,018 (for women))
Extra renal support requirement defined by percentage of patients requiring at least one dialysis
Extra renal support requirement
Kidney function measured by serum creatinine value
Kidney function measured by serum creatinine value
Kidney function measured by CKD EPI
Kidney function measured by CKD EPI (= 141 x min(Scr/K,1)a x max(Scr/K,1)-1,209 x 0,993Age x 1,018 (for women))
Extra renal support requirement defined by percentage of patients requiring at least one dialysis
Extra renal support requirement

Full Information

First Posted
February 15, 2017
Last Updated
June 17, 2022
Sponsor
Nantes University Hospital
Collaborators
Ministry of Health, France
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1. Study Identification

Unique Protocol Identification Number
NCT03098706
Brief Title
Therapeutic Hypothermia in "Expanded Criteria" Brain-dead Donors and Kidney-graft Function
Acronym
HYPOREME
Official Title
Impact of Therapeutic Hypothermia in Expanded Criteria Brain-dead Donors on Kidney-graft Function in the Kidney-transplant Recipients: Multicenter Randomized Controlled Trial" HYPOREME
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
November 8, 2017 (Actual)
Primary Completion Date
March 21, 2022 (Actual)
Study Completion Date
March 21, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nantes University Hospital
Collaborators
Ministry of Health, France

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Each year, only one third of patients registered on the waiting list receive a kidney transplant. Numerous paths are being explored with the aim of reversing this shortage. The first is to increase the number of organs by developing harvesting from donors in a state of brain-death (BD) termed "expanded criteria donors" or from patients deceased from circulatory arrest. Another fundamental factor is to insure the success of the transplant by limiting the dysfunction of donor kidneys, marked by a delayed graft function (DFG). The development of techniques to insure correct perfusion of harvested organs, and the optimization of reanimation and intensive care of brain-dead donors constitute important factors in DGF reduction. Therapeutic Hypothermia could to be an attractive care strategy for BD patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Organ Donor, Brain Death, Kidney Transplant; Complications, Critical Illness, Hypothermia

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
532 (Actual)

8. Arms, Groups, and Interventions

Arm Title
NT normothermia
Arm Type
Other
Arm Description
After information for donation and research has been explained, organ donors in the normothermia (NT) group will either be maintained to spontaneously reach a body temperature of 36,5 °C-37,5°, until transfer to the operating room.
Arm Title
HT mild hypothermia
Arm Type
Experimental
Arm Description
The intervention will take place after information for donation and research has been explained . Organ donors in the intervention group will either be actively warmed or allowed to reach a body temperature of 34 °C-35°C, until transfer to the operating room.
Intervention Type
Procedure
Intervention Name(s)
Procedure control: normothermia
Other Intervention Name(s)
Normothermia
Intervention Description
Temperature will be maintained between 36.5° and 37.5°C in the control group. In case of temperature superior to 37.5°C or inferior to 36.5°C, a pharmaceutical treatment and/or active cooling or warming will be introduce to maintain temperature between the range of 36.5 - 37.5°C.
Intervention Type
Procedure
Intervention Name(s)
Procedure active
Other Intervention Name(s)
Therapeutic hypothermia/ Induce hypothermia
Intervention Description
Therapeutic hypothermia ie targeted controlled temperature between 34° and 35°C will be induced in the active group. Usual method of controlled temperature will be used in ICU: internal active method or external active method.
Primary Outcome Measure Information:
Title
rate of patients with delayed graft function (DGF)
Description
DGF is the recipient's requirement for dialysis during the first week after transplantation. To show the interest of Targeted Temperature Management in order to optimize the functional recovery of transplanted kidney transplants by comparing 2 groups of recipient subjects: those receiving one Graft from an "expanded criteria donors" maintained in hypothermia (34°-35°) and those receiving a graft from an "expanded criteria donors" maintained in normothermia (36,5°-37,5°).
Time Frame
Day 7
Secondary Outcome Measure Information:
Title
Temperature Profile
Description
comparison of temperature profile between the two arms
Time Frame
24 hours
Title
Severe arrhythmias
Description
Severe arrythmia will be define by salvo of ventricular extrasystole, ventricular fibrillation, ventricular tachycardia, need an external shock, need anti-arrhythmic treatment. Participants will be followed for the duration of Intensive Care Unit stay and/or operating room, an expected average of 24 hours.
Time Frame
24 hours
Title
Cardiac arrest
Description
SParticipants will be followed for the duration of Intensive Care Unit stay and/or operating room, an expected average of 24 hours.
Time Frame
24 hours
Title
Occurrence of hypotension measured by Total dose of inotropic drugs
Description
Total dose of different inotropic drugs (Epinephrine, Norepinephrine, Dobutamine) will be compare between 2 groups during targetted controlled temperature management period.
Time Frame
24 hours
Title
Occurrence of hypotension measured by cumulative fluid balance
Description
Cumulative fluid balance will be compare between 2 groups during targetted controlled temperature management period
Time Frame
24 hours
Title
occurrence of cardiac arrest
Description
comparison of occurrence of cardiac arrest between the two arms
Time Frame
24 hours
Title
Kidney function measured by serum creatinine value
Description
Kidney function measured by serum creatinine value
Time Frame
24 hours
Title
Kidney function measured by CKD EPI score
Description
Kidney function measured by CKD EPI score (= 141 x min(Scr/K,1)a x max(Scr/K,1)-1,209 x 0,993Age x 1,018 (for women))
Time Frame
24 hours
Title
electrolyte balance : potassium, calcium, sodium concentration disorders in mmoL/L
Description
Potential hypothermia related side effects
Time Frame
24hours
Title
glycemia in mmoL/L
Description
Potential hypothermia related side effects
Time Frame
24hours
Title
liver disorder (ASAT, ALAT, GGT, PAL , BILI in UI/L )
Description
Potential hypothermia related side effects
Time Frame
24hours
Title
thrombocytopenia in mm3/L
Description
Potential hypothermia related side effects
Time Frame
24hours
Title
Number of individual organs transplanted
Description
Participants will be followed for the duration of Intensive care unit length of stay, and operating room, an average of 24 hours.
Time Frame
24 hours
Title
Hospital mortality
Description
Participants will be followed for the duration of hospital stay, an expected average of 1 week.
Time Frame
Day 7
Title
Kidney function measured by serum creatinine value
Description
Kidney function measured by serum creatinine value at day7
Time Frame
Day 7
Title
Kidney function measured by CKD EPI
Description
Kidney function measured by CKD EPI (= 141 x min(Scr/K,1)a x max(Scr/K,1)-1,209 x 0,993Age x 1,018 (for women))
Time Frame
Day 7
Title
Extra renal support requirement
Description
Extra renal support requirement at Day7
Time Frame
Day 7
Title
Kidney graft acute rejection
Description
Kidney graft acute rejection
Time Frame
Day 7
Title
Acute pulmonary oedema by left ventricular failure
Description
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days.
Time Frame
Day 7
Title
Severe arrythmia
Description
Severe arrythmia will be define by salvo of ventricular extrasystole, ventricular fibrillation, ventricular tachycardia, need an external shock, need anti-arrhythmic treatment. Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Time Frame
Day 7
Title
Pulmonary embolism
Description
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Time Frame
Day 7
Title
Acute coronary syndrome
Description
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Time Frame
Day 7
Title
Nosocomial Bloodstream infection
Description
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Time Frame
Day 7
Title
Early onset pneumonia
Description
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Time Frame
Day 7
Title
Central Venous Catheter infection
Description
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Time Frame
Day 7
Title
Urinary tract sepsis
Description
Participants will be followed for the duration of transplantation unit stay, an expected average of 7 days
Time Frame
Day 7
Title
Mortality at D28
Description
comparison of mortality at D28 between the two arms
Time Frame
D28
Title
Mortality at 3 months
Description
comparison of mortality at 3months between the two arms
Time Frame
3 months
Title
Mortality at 1 year
Description
comparison of mortality at 1 year between the two arms
Time Frame
1 year
Title
Length of hospital stay
Description
comparison of length of hospital stay between the two arms
Time Frame
48months
Title
Kidney function measured by serum creatinine value
Description
Kidney function measured by serum creatinine value
Time Frame
D28
Title
Kidney function measured by CKD EPI
Description
Kidney function measured by CKD EPI (= 141 x min(Scr/K,1)a x max(Scr/K,1)-1,209 x 0,993Age x 1,018 (for women)) at Day28
Time Frame
D28
Title
Extra renal support requirement defined by percentage of patients requiring at least one dialysis
Description
Extra renal support requirement
Time Frame
D28
Title
Kidney graft acute rejection
Description
Kidney graft acute rejection
Time Frame
D28
Title
Acute pulmonary oedema by left ventricular failure
Description
Acute pulmonary oedema by left ventricular failure
Time Frame
D28
Title
Severe arrythmia
Description
Severe arrythmia will be define by salvo of ventricular extrasystole, ventricular fibrillation, ventricular tachycardia, need an external shock, need anti-arrhythmic treatment.
Time Frame
D28
Title
Pulmonary embolism
Description
Pulmonary embolism
Time Frame
D28
Title
Acute coronary syndrome
Description
Acute coronary syndrome
Time Frame
D28
Title
Nosocomial Bloodstream infection
Description
Nosocomial Bloodstream infection
Time Frame
D28
Title
Early onset pneumonia
Description
Early onset pneumonia
Time Frame
D28
Title
Central Venous Catheter infection
Description
Central Venous Catheter infection
Time Frame
D28
Title
Urinary tract sepsis
Description
Urinary tract sepsis
Time Frame
D28
Title
Kidney function measured by serum creatinine value
Description
Kidney function measured by serum creatinine value
Time Frame
3 months
Title
Kidney function measured by CKD EPI
Description
Kidney function measured by CKD EPI (= 141 x min(Scr/K,1)a x max(Scr/K,1)-1,209 x 0,993Age x 1,018 (for women))
Time Frame
3 months
Title
Extra renal support requirement defined by percentage of patients requiring at least one dialysis
Description
Extra renal support requirement
Time Frame
3 months
Title
Kidney function measured by serum creatinine value
Description
Kidney function measured by serum creatinine value
Time Frame
12 months
Title
Kidney function measured by CKD EPI
Description
Kidney function measured by CKD EPI (= 141 x min(Scr/K,1)a x max(Scr/K,1)-1,209 x 0,993Age x 1,018 (for women))
Time Frame
12 months
Title
Extra renal support requirement defined by percentage of patients requiring at least one dialysis
Description
Extra renal support requirement
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: For donors: legal determination of death by neurologic criteria/deceased organ donor/no medical contre-indication to donation/Information given to the authorizing surrogate/ Pregnant women. For transplant recipients : age 18 years or greater /information given and no opposition signed by recipients. Exclusion Criteria: For donors: no legal determination of death by neurologic criteria/not a deceased organ donor/ medical contre-indication to donation/ no Information given to the authorizing surrogate. For transplant recipients: age <18 years / no information given and/or opposition signed by recipients.
Facility Information:
Facility Name
CHU Amiens-Picardie
City
Amiens
ZIP/Postal Code
80054
Country
France
Facility Name
CHU d'Angers
City
Angers
ZIP/Postal Code
49000
Country
France
Facility Name
CH Angouleme
City
Angoulême
ZIP/Postal Code
16959
Country
France
Facility Name
CH Avignon
City
Avignon
ZIP/Postal Code
84000
Country
France
Facility Name
CH de Blois
City
Blois
ZIP/Postal Code
41016
Country
France
Facility Name
CHU de Bordeaux
City
Bordeaux
ZIP/Postal Code
33076
Country
France
Facility Name
CH Bourges
City
Bourges
ZIP/Postal Code
18020
Country
France
Facility Name
CHU Brest
City
Brest
ZIP/Postal Code
29200
Country
France
Facility Name
CHU Caen
City
Caen
ZIP/Postal Code
14000
Country
France
Facility Name
Ch Cholet
City
Cholet
ZIP/Postal Code
49325
Country
France
Facility Name
Chu Clermont Ferrand
City
Clermont-Ferrand
Country
France
Facility Name
Hopital Henri Mondor
City
Créteil
ZIP/Postal Code
94000
Country
France
Facility Name
CHU de Dijon
City
Dijon
ZIP/Postal Code
21079
Country
France
Facility Name
CH de Dreux
City
Dreux
ZIP/Postal Code
28100
Country
France
Facility Name
CHU Grenoble
City
Grenoble
Country
France
Facility Name
CH Marne la Vallée (GHEF)
City
Jossigny
ZIP/Postal Code
77600
Country
France
Facility Name
CH La Roche sur Yon
City
La Roche-sur-Yon
ZIP/Postal Code
85925
Country
France
Facility Name
CH La Rochelle
City
La Rochelle
ZIP/Postal Code
17019
Country
France
Facility Name
CH Laval
City
Laval
ZIP/Postal Code
53000
Country
France
Facility Name
Hopital Bicetre
City
Le Kremlin-Bicêtre
ZIP/Postal Code
94270
Country
France
Facility Name
CH Le Mans
City
Le Mans
ZIP/Postal Code
72037
Country
France
Facility Name
CHRU Lille
City
Lille
ZIP/Postal Code
59000
Country
France
Facility Name
CHU Limoges
City
Limoges
ZIP/Postal Code
87042
Country
France
Facility Name
CH Lorient
City
Lorient
ZIP/Postal Code
56322
Country
France
Facility Name
CHU de Lyon
City
Lyon
Country
France
Facility Name
Hopital de la Conception
City
Marseille
ZIP/Postal Code
13005
Country
France
Facility Name
Hopital de la Timone
City
Marseille
ZIP/Postal Code
13005
Country
France
Facility Name
CH de Meaux (GHEF)
City
Meaux
Country
France
Facility Name
CHU Montpellier
City
Montpellier
Country
France
Facility Name
CH Morlaix
City
Morlaix
ZIP/Postal Code
29672
Country
France
Facility Name
Nantes University Hospital
City
Nantes
ZIP/Postal Code
44093
Country
France
Facility Name
CHU Nice
City
Nice
ZIP/Postal Code
06000
Country
France
Facility Name
CH Orléans
City
Orléans
ZIP/Postal Code
45067
Country
France
Facility Name
Hopital Saint Louis
City
Paris
ZIP/Postal Code
75010
Country
France
Facility Name
Hopital de la Pitié Salpetriere
City
Paris
ZIP/Postal Code
75013
Country
France
Facility Name
Hopital Necker
City
Paris
ZIP/Postal Code
75015
Country
France
Facility Name
CHU Tenon
City
Paris
ZIP/Postal Code
75020
Country
France
Facility Name
CHU Poitiers
City
Poitiers
ZIP/Postal Code
86000
Country
France
Facility Name
CH Annecy Genevois
City
Pringy
ZIP/Postal Code
74374
Country
France
Facility Name
CH Cornouaille
City
Quimper
ZIP/Postal Code
29107
Country
France
Facility Name
CHU Reims
City
Reims
ZIP/Postal Code
51100
Country
France
Facility Name
CHU Rennes
City
Rennes
ZIP/Postal Code
35000
Country
France
Facility Name
CHU Rouen
City
Rouen
ZIP/Postal Code
76000
Country
France
Facility Name
CH Saint Brieuc
City
Saint Brieuc
ZIP/Postal Code
22027
Country
France
Facility Name
CH Saint Nazaire
City
Saint Nazaire
ZIP/Postal Code
44606
Country
France
Facility Name
CH Saint Malo
City
Saint-Malo
ZIP/Postal Code
35403
Country
France
Facility Name
CHRU Saint-Etienne
City
Saint-Étienne
ZIP/Postal Code
42055
Country
France
Facility Name
CH Saintes
City
Saintes
ZIP/Postal Code
17108
Country
France
Facility Name
CHU Strasbourg
City
Strasbourg
ZIP/Postal Code
67091
Country
France
Facility Name
CHU Foch
City
Suresnes
ZIP/Postal Code
92150
Country
France
Facility Name
CHU Toulouse
City
Toulouse
ZIP/Postal Code
31403
Country
France
Facility Name
CHU Tours
City
Tours
ZIP/Postal Code
37044
Country
France
Facility Name
CHRU Nancy
City
Vandœuvre-lès-Nancy
ZIP/Postal Code
54511
Country
France
Facility Name
CH Vannes
City
Vannes
ZIP/Postal Code
56000
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
35351701
Citation
Brule N, Canet E, Pere M, Feuillet F, Hourmant M, Asehnoune K, Rozec B, Duveau A, Dube L, Pierrot M, Humbert S, Tirot P, Boyer JM, Martin-Lefevre L, Labadie F, Robert R, Benard T, Kerforne T, Thierry A, Lesieur O, Vincent JF, Lesouhaitier M, Larmet R, Vigneau C, Goepp A, Bouju P, Quentin C, Egreteau PY, Huet O, Renault A, Le Meur Y, Venhard JC, Buchler M, Michel O, Voellmy MH, Herve F, Schnell D, Courte A, Glotz D, Amrouche L, Hazzan M, Kamar N, Moal V, Bourenne J, Le Quintrec-Donnette M, Morelon E, Boulain T, Grimbert P, Heng AE, Merville P, Garin A, Hiesse C, Fermier B, Mousson C, Guyot-Colosio C, Bouvier N, Rerolle JP, Durrbach A, Drouin S, Caillard S, Frimat L, Girerd S, Albano L, Rostaing L, Bertrand D, Hertig A, Westeel PF, Montini F, Delpierre E, Dorez D, Alamartine E, Ouisse C, Sebille V, Reignier J. Impact of targeted hypothermia in expanded-criteria organ donors on recipient kidney-graft function: study protocol for a multicentre randomised controlled trial (HYPOREME). BMJ Open. 2022 Mar 28;12(3):e052845. doi: 10.1136/bmjopen-2021-052845.
Results Reference
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Therapeutic Hypothermia in "Expanded Criteria" Brain-dead Donors and Kidney-graft Function

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