Early Deresuscitation Strategy Driven by Tissue Perfusion in Renal Replacement Therapy in Patients With Acute Renal Failure
Condition(s) studied
Investigational drug(s) / intervention(s)
Fluid balance negativation: During the RRT, UFnet will be settled on 2ml/kg/h and adapted to hemodynamic tolerance and tissue perfusion . When the patient's baseline body weight is reached the UF net will be settled to maintain it. In case of failure of the fluid balance negativation after 24h, UFnet will be settled on 3ml/kg/h. Then when the baseline body weight is reached UFnet will be settled on 0.5 et 1ml/kg/h or if necessary adapted to 1,5ml/kg/h to maintain it In case of hemodynamic intolerance (NADN \> 0,5 µg/kg/min) or tissue hypoperfusion, UF net will be stopped during 6 hours and restarted if NADN \< 0,5 µg/kg/min and without tissue hypoperfusion.
Body weight Stabilization: During the RRT, UFnet will be settled between 0 et 1 ml/kg/h and adapted in case of weight stabilization failure or hemodynamic intolerance. In case of weight stabilisation failure ( variation \>3% after 24h), the UF net can be increased to 1,5 ml/kg/h, as long as high intakes require UFnette at 1.5mL/kg/h to stabilize water balance, with daily reassessment. In case of hemodynamic intolerance (NADN \> 0,5 µg/kg/min), UF net will be stopped during 6 hours and restarted if NADN \< 0,5 µg/kg/min.
Study summary
In Intensive Care Unit (ICU) patients with acute kidney injury (AKI) and treated with renal replacement therapy (RRT) often present a fluid overload which is associated with morbidity (mechanical ventilation duration increase, kidney recovery decrease) and mortality.
Patients' prognostic could be improved by correcting the fluid overload with net ultrafiltration (UFnet) however it may lead to harmful iatrogenic hypovolemia responsible of deleterious ischemic lesions.
In usual practice, UF net prescription are variable and there are different international recommendations. Some observational studies suggest that using a UFnet between 1 et 1.75 mL/kg/h in fluid overloaded patient decrease mortality.
Fluid overload increases morbidity and mortality, particularly in RRT. Studies without RRT argue for an efficacy of management by decreasing the fluid overload .Cohort studies suggest to use a moderate UFnet instead of a low UFnet. Some data from studies on early versus late RRT that relate the fluid balance or correct the fluid overload during the early strategy argue for a beneficial effect of an early deresuscitation strategy
Consequently, the impact of a moderate UFnet (to decrease the fluid overload) compared to a low UFnet (to stabilize the fluid overload) in a randomized interventional study could be assessed.
The study hypothesis is that :
an early fluid overload deresuscitation protocol with a high UFnet (2 ml/kg/h) targeting both the negativation of cumulated fluid balance to reach a dry weight and the maintenance of tissue perfusion.
Compared to
fluid overload deresuscitation protocol with a low UFnet (between 0 and 1 ml/kg/h) to reach a stabilization of cumulated fluid balance without monitoring the tissue perfusion.
could improve overall, renal, hemodynamic and respiratory prognosis in fluid overloaded patients with renal replacement therapy in ICU
Eligibility
Primary outcome measure(s)
- Number of organ replacement free-days — Day 30
Number of organ replacement free-days, i.e, number of renal replacement therapy-free days, number of vasopressor-free days, number of ventilator-free day. Number of days between 2 same type organ replacement interruption is not counted. In case of death before 30 days, number of days is censored to 0.
Trial sites (14)
| Facility | City | Region | Status |
|---|---|---|---|
| Centre Hospitalier d'Ajaccio | Ajaccio | France | Not Yet Recruiting |
| CHU Amiens-Picardie | Amiens | France | Not Yet Recruiting |
| Service d'Anesthesie-Réanimation, Hôpital Louis Pradel, Hospices Civils de Lyon | Bron | France | Recruiting |
| CHU Caen Normandie | Caen | France | Not Yet Recruiting |
| Service de Réanimation, CHU de Dijon | Dijon | France | Recruiting |
| GHP Saint Joseph Marie Lannelongue | Le Plessis-Robinson | France | Not Yet Recruiting |
| CHU Lille - Hôpital Roger Salengro | Lille | France | Not Yet Recruiting |
| Hôpital Edouard Herriot, Groupement Hospitalier Centre | Lyon | France | Recruiting |
| Hôpital de la Croix Rousse | Lyon | France | Not Yet Recruiting |
| Hôpital de la Croix Rousse | Lyon | France | Recruiting |
| Service de Réanimation, Clinique de la Sauvegarde | Lyon | France | Recruiting |
| Hôpital Edouard Herriot | Lyon | France | Not Yet Recruiting |
| Département d'anesthésie réanimation Hôpital Européen Georges Pompidou | Paris | France | Recruiting |
| Hôpitaux de Bradois - CHRU Nancy | Vandœuvre-lès-Nancy | France | Not Yet Recruiting |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05817539 on ClinicalTrials.gov ↗ ← All trials in France