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Plasmalyte Versus Saline in Trauma Patients (ASTRAU)

Primary Purpose

Severe Trauma Patients, Acute Kidney Injury

Status
Recruiting
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Plasmalyte Viaflo
NaCl 0.9%
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Severe Trauma Patients focused on measuring Severe trauma, Acute kidney injury, Fluid resuscitation, Sodium chloride, Plasmalyte

Eligibility Criteria

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

Inclusion Criteria:

  • Severe trauma defined by at least one Vittel criteria
  • Prescription for at least one red blood cell unit transfusion within 6 hours after trauma
  • Delay between trauma and study randomization ≤ 6 hours
  • Patient able to give consent or included in emergency situation
  • Patient affiliated to Health security system

Exclusion Criteria:

  • Age < 18 years
  • Chronic kidney disease needing requiring renal replacement therapy
  • Participation to another interventional trial interacting with renal function or which requires the use of a fluid resuscitation
  • Fluid resuscitation > 4000 mL before inclusion

Sites / Locations

  • Département d'Anesthésie Réanimation - Kremlin BicêtreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Plasmalyte Viaflo

NaCl 0.9%

Arm Description

Intervention type: drug (Plasmalyte Viaflo) Intervention name: plasmalyte Intervention description: fluid resuscitation using exclusively Plasmalyte up to 20L during the first 5 days

Intervention type: drug (NaCl 0.9%) Intervention name: NaCl 0.9% Intervention description: fluid resuscitation using exclusively NaCl 0.9% up to 20L during the first 5 days

Outcomes

Primary Outcome Measures

Proportion of Acute Kidney Injury (stage 2 or 3 according to KDIGO classification) over the 5 first days after trauma

Secondary Outcome Measures

Proportion of patients requiring renal replacement therapy (during 28 days)
Amount of transfused blood product units (during the first 5 days)
Number of days alive without free of mechanical ventilation (during 28 days)
Days spent alive outside the ICU (during 28 days)
Mortality
Difference between the serum creatinine peak in the 5 first days of ICU stay and the baseline creatinine

Full Information

First Posted
August 10, 2018
Last Updated
December 7, 2022
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT03630224
Brief Title
Plasmalyte Versus Saline in Trauma Patients
Acronym
ASTRAU
Official Title
Renal Effects of Fluid Resuscitation With Plasmalyte Viaflo Versus Saline in Trauma Patients (the ASTRAU Study)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 24, 2019 (Actual)
Primary Completion Date
July 24, 2024 (Anticipated)
Study Completion Date
July 24, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

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
Fluid resuscitation remains the cornerstone for the care of severe trauma patients to compensate for blood loss, to compensate for capillary leak induced by systemic inflammation but also to prevent the detrimental consequences of traumatic rhabdomyolysis. Isotonic saline (NaCl 0.9%), called "physiological serum" is the standard fluid for the resuscitation of severely injured patients. However, the formulation of NaCl 0.9% is not really physiological since its chloride concentration is 1.5 higher than the one of human plasma. This excessive chloride concentration leads to hyperchloremic acidosis and to a drop in renal perfusion after isotonic saline infusion. For this reason, we wonder whether fluid resuscitation with Plasmalyte would be beneficial for renal function of trauma patients in comparison with NaCl 0.9%. Our research question is: In a population of trauma patients at high risk of acute kidney injury, does a fluid resuscitation with Plasmalyte Viaflo lower the incidence of severe acute kidney injury (stage 2 or 3 according to the KDIGO classification) compared with a resuscitation with isotonic saline (NaCl 0.9%)?
Detailed Description
Fluid resuscitation remains the cornerstone for the care of severe trauma patients to compensate for blood loss, to compensate for capillary leak induced by systemic inflammation but also to prevent the detrimental consequences of traumatic rhabdomyolysis. Isotonic saline (NaCl 0.9%), called "physiological serum" is the standard fluid for the resuscitation of severely injured patients. However, the formulation of NaCl 0.9% is not really physiological since its chloride concentration is 1.5 higher than plasma. This excessive chloride concentration leads to hyperchloremic acidosis and to a drop in renal perfusion after isotonic saline infusion. A retrospective study conducted in the perioperative setting (abdominal surgery) reported a significant decrease in mortality and acute kidney injury in 926 patients receiving balanced crystalloid solution compared to a propensity-matched population of 2778 patients receiving isotonic saline. Yunos et al. conducted a prospective sequential period study including 760 patients receiving chloride-rich solution during the first 6-month period and 773 patients receiving chloride-poor solution during the next 6-month period. They reported a decrease in severe acute kidney injury (I or F in the RIFLE classification) in the group receiving chloride-poor solution. Large retrospective studies in intensive care confirmed a beneficial effect of the use of chloride-poor solutions on survival compared to chloride-rich solutions. A recent meta-analysis including 5 small size randomized controlled trials, 1 controlled trial and two retrospective studies, reported also a decrease in acute kidney injury. A recent multicenter study randomized 2778 patients to receive either Plasmalyte 148 or NaCl 0.9% during their ICU stay. No AKI or mortality differences were reported. However, this study included patients with low ICU severity score (mean APACHE II = 14) and at low risk of severe AKI (severe AKI incidence = 9%). Moreover, they received a median amount of fluid of 2000 mL during their ICU stay. This small fluid volume may not be enough to show any difference between rich-chloride and poor-chloride solutions on AKI in this population with low ICU severity scores. Trauma patients are particularly at risk of AKI during the acute phase of trauma because of hypovolemia (bleeding), rhabdomyolysis and systemic inflammation (traumatic tissue injuries and emergency surgeries). AKI is reported in 18 to 26 % of trauma patients. In our database (TraumaBase®, traumabase.eu) that included at the time of the study the 6 trauma centers of the Paris area (France), we reported a 24% incidence of severe AKI (stage I or F of the RIFLE classification) in the subpopulation of patients needing at least one red blood cell unit transfusion in the 6 first hours of care. Moreover, this subpopulation receives an average amount of 6000 mL of fluid during the first 24 hours of care. We postulate that trauma patients at high risk of AKI receiving high volume of fluid can be the best population target to demonstrate a beneficial effect of Plasmalyte vs isotonic saline on severe AKI occurrence in a prospective, blinded, randomized manner. Thus, we formulate the following hypothesis: In a population of trauma patients, at high risk of AKI, a fluid resuscitation with Plasmalyte Viaflo during the 5 first days of care will lower decrease the incidence of severe acute kidney injury (stage 2 or 3 according to the KDIGO classification) compared with a resuscitation with isotonic saline (NaCl 0.9%)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Trauma Patients, Acute Kidney Injury
Keywords
Severe trauma, Acute kidney injury, Fluid resuscitation, Sodium chloride, Plasmalyte

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
622 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Plasmalyte Viaflo
Arm Type
Experimental
Arm Description
Intervention type: drug (Plasmalyte Viaflo) Intervention name: plasmalyte Intervention description: fluid resuscitation using exclusively Plasmalyte up to 20L during the first 5 days
Arm Title
NaCl 0.9%
Arm Type
Active Comparator
Arm Description
Intervention type: drug (NaCl 0.9%) Intervention name: NaCl 0.9% Intervention description: fluid resuscitation using exclusively NaCl 0.9% up to 20L during the first 5 days
Intervention Type
Drug
Intervention Name(s)
Plasmalyte Viaflo
Intervention Description
Intervention description: fluid resuscitation using exclusively Plasmalyte up to 20L during the first 5 days
Intervention Type
Drug
Intervention Name(s)
NaCl 0.9%
Intervention Description
Intervention name: NaCl 0.9% Intervention description: fluid resuscitation using exclusively NaCl 0.9% up to 20L during the first 5 days
Primary Outcome Measure Information:
Title
Proportion of Acute Kidney Injury (stage 2 or 3 according to KDIGO classification) over the 5 first days after trauma
Time Frame
over the 5 first days after trauma
Secondary Outcome Measure Information:
Title
Proportion of patients requiring renal replacement therapy (during 28 days)
Time Frame
during 28 days
Title
Amount of transfused blood product units (during the first 5 days)
Time Frame
during the first 5 days
Title
Number of days alive without free of mechanical ventilation (during 28 days)
Time Frame
during 28 days
Title
Days spent alive outside the ICU (during 28 days)
Time Frame
during 28 days
Title
Mortality
Time Frame
at 28 days
Title
Difference between the serum creatinine peak in the 5 first days of ICU stay and the baseline creatinine
Time Frame
during the 5 first days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Severe trauma defined by at least one Vittel criteria Prescription for at least one red blood cell unit transfusion within 6 hours after trauma Delay between trauma and study randomization ≤ 6 hours Patient able to give consent or included in emergency situation Patient affiliated to Health security system Exclusion Criteria: Age < 18 years Chronic kidney disease needing requiring renal replacement therapy Participation to another interventional trial interacting with renal function or which requires the use of a fluid resuscitation Fluid resuscitation > 4000 mL before inclusion
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Anatole HARROIS, MD
Phone
+33(0)145213441
Email
harroisanatole@yahoo.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Jacques DURANTEAU, MD, PhD
Email
jacques.duranteau@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anatole HARROIS
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Département d'Anesthésie Réanimation - Kremlin Bicêtre
City
Le Kremlin-Bicêtre
ZIP/Postal Code
94270
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anatole HARROIS, MD

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
22580944
Citation
Chowdhury AH, Cox EF, Francis ST, Lobo DN. A randomized, controlled, double-blind crossover study on the effects of 2-L infusions of 0.9% saline and plasma-lyte(R) 148 on renal blood flow velocity and renal cortical tissue perfusion in healthy volunteers. Ann Surg. 2012 Jul;256(1):18-24. doi: 10.1097/SLA.0b013e318256be72. Erratum In: Ann Surg. 2013 Dec;258(6):1118.
Results Reference
background
PubMed Identifier
22470070
Citation
Shaw AD, Bagshaw SM, Goldstein SL, Scherer LA, Duan M, Schermer CR, Kellum JA. Major complications, mortality, and resource utilization after open abdominal surgery: 0.9% saline compared to Plasma-Lyte. Ann Surg. 2012 May;255(5):821-9. doi: 10.1097/SLA.0b013e31825074f5.
Results Reference
background
PubMed Identifier
23073953
Citation
Yunos NM, Bellomo R, Hegarty C, Story D, Ho L, Bailey M. Association between a chloride-liberal vs chloride-restrictive intravenous fluid administration strategy and kidney injury in critically ill adults. JAMA. 2012 Oct 17;308(15):1566-72. doi: 10.1001/jama.2012.13356.
Results Reference
background
PubMed Identifier
25293535
Citation
Shaw AD, Raghunathan K, Peyerl FW, Munson SH, Paluszkiewicz SM, Schermer CR. Association between intravenous chloride load during resuscitation and in-hospital mortality among patients with SIRS. Intensive Care Med. 2014 Dec;40(12):1897-905. doi: 10.1007/s00134-014-3505-3. Epub 2014 Oct 8.
Results Reference
background
PubMed Identifier
24674927
Citation
Raghunathan K, Shaw A, Nathanson B, Sturmer T, Brookhart A, Stefan MS, Setoguchi S, Beadles C, Lindenauer PK. Association between the choice of IV crystalloid and in-hospital mortality among critically ill adults with sepsis*. Crit Care Med. 2014 Jul;42(7):1585-91. doi: 10.1097/CCM.0000000000000305.
Results Reference
background
PubMed Identifier
26370823
Citation
Shaw AD, Schermer CR, Lobo DN, Munson SH, Khangulov V, Hayashida DK, Kellum JA. Impact of intravenous fluid composition on outcomes in patients with systemic inflammatory response syndrome. Crit Care. 2015 Sep 12;19(1):334. doi: 10.1186/s13054-015-1045-z. Erratum In: Crit Care. 2016;20:17.
Results Reference
background
PubMed Identifier
25357011
Citation
Krajewski ML, Raghunathan K, Paluszkiewicz SM, Schermer CR, Shaw AD. Meta-analysis of high- versus low-chloride content in perioperative and critical care fluid resuscitation. Br J Surg. 2015 Jan;102(1):24-36. doi: 10.1002/bjs.9651. Epub 2014 Oct 30.
Results Reference
background
PubMed Identifier
26444692
Citation
Young P, Bailey M, Beasley R, Henderson S, Mackle D, McArthur C, McGuinness S, Mehrtens J, Myburgh J, Psirides A, Reddy S, Bellomo R; SPLIT Investigators; ANZICS CTG. Effect of a Buffered Crystalloid Solution vs Saline on Acute Kidney Injury Among Patients in the Intensive Care Unit: The SPLIT Randomized Clinical Trial. JAMA. 2015 Oct 27;314(16):1701-10. doi: 10.1001/jama.2015.12334. Erratum In: JAMA. 2015 Dec 15;314(23):2570.
Results Reference
background
PubMed Identifier
18661407
Citation
Bagshaw SM, George C, Gibney RT, Bellomo R. A multi-center evaluation of early acute kidney injury in critically ill trauma patients. Ren Fail. 2008;30(6):581-9. doi: 10.1080/08860220802134649.
Results Reference
background
PubMed Identifier
20562612
Citation
Bihorac A, Delano MJ, Schold JD, Lopez MC, Nathens AB, Maier RV, Layon AJ, Baker HV, Moldawer LL. Incidence, clinical predictors, genomics, and outcome of acute kidney injury among trauma patients. Ann Surg. 2010 Jul;252(1):158-65. doi: 10.1097/SLA.0b013e3181deb6bc.
Results Reference
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Plasmalyte Versus Saline in Trauma Patients

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