Acute Kidney Injury Clinical Trial
— ASTRAUOfficial title:
Renal Effects of Fluid Resuscitation With Plasmalyte Viaflo Versus Saline in Trauma Patients (the ASTRAU Study)
| Verified date | January 2024 |
| Source | Assistance Publique - Hôpitaux de Paris |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
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%)?
| Status | Terminated |
| Enrollment | 365 |
| Est. completion date | August 18, 2023 |
| Est. primary completion date | August 18, 2023 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | 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 |
| Country | Name | City | State |
|---|---|---|---|
| France | Département d'Anesthésie Réanimation - Kremlin Bicêtre | Le Kremlin-Bicêtre |
| Lead Sponsor | Collaborator |
|---|---|
| Assistance Publique - Hôpitaux de Paris |
France,
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| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Proportion of Acute Kidney Injury (stage 2 or 3 according to KDIGO classification) over the 5 first days after trauma | over the 5 first days after trauma | ||
| Secondary | Proportion of patients requiring renal replacement therapy (during 28 days) | during 28 days | ||
| Secondary | Amount of transfused blood product units (during the first 5 days) | during the first 5 days | ||
| Secondary | Number of days alive without free of mechanical ventilation (during 28 days) | during 28 days | ||
| Secondary | Days spent alive outside the ICU (during 28 days) | during 28 days | ||
| Secondary | Mortality | at 28 days | ||
| Secondary | Difference between the serum creatinine peak in the 5 first days of ICU stay and the baseline creatinine | during the 5 first days |
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