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Can a diuretic plan clear excess fluid in critically ill patients?
NCT ID NCT02345681
First seen Sep 14, 2026 · Last updated Sep 15, 2026 · Updated 1 time
Summary
Critically ill patients in the intensive care unit often accumulate too much fluid, which can lead to complications. This trial tests whether a furosemide-based algorithm can safely reduce fluid overload in patients who are on mechanical ventilation and have gained at least 3% of their body weight. Researchers will compare fluid balance and outcomes like ventilator-free days and ICU stay between patients who receive the algorithm and those who do not.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- furosemide, a diuretic that helps the body remove excess fluid
- What this could lead to
- If it works, this could give ICU doctors a clear, step-by-step way to use diuretics to reduce fluid buildup, potentially shortening time on a ventilator and stay in intensive care.
- What could go wrong
- Diuretics can cause dehydration, kidney problems, or low blood pressure, especially in very sick patients. The trial is small and early, so the approach may not work or may not be safe for all ICU patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
171 people
The number who actually took part.
- Started
-
May 2015
- Finished
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Apr 2019
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age of 18 or more * Patients receiving endo-tracheal intubation and mechanical ventilation during their stay in the ICU * Weight increase of at least 3 % during the stay. Baseline weight is regarded as the weight at the 24th hour after ICU admission * FiO2 \< 60 %, PEEP \< 10cmH20 * No administration of catecholamines other than dobutamine at a dose of 10 microg.Kg-1.min-1 Exclusion Criteria: * Pregnancy * Patient with a moribund state at ICU arrival * Acute brain injury (traumatic brain injury, subarachnoid hemorrhage, intra-cerebral bleeding, stroke, meningo-encephalitis, coma from medication origin) * Chronic kidney disease defined as creatinin clearance \< 30mL.min-1 and/or with chronic dialysis * Mandatory administration of diuretics (cardiogenic pulmonary oedema, LVEF \< 30 %)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
CHD Vendée
La Roche-sur-Yon, France
-
CHU de Nantes
Nantes, 44093, France
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Hôpital François Mitterand
Dijon, France
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Other studies related to the condition(s) this trial covers.
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