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NCT07625995
Feasibility and Safety of Targeting Neutral vs Liberal Fluid Balance in Traumatic Brain Injured Patients- LIMIT-TBI Trial
Conditions: Traumatic Brain Injury, Severe Traumatic Brain Injury, Acute Brain Injury, Neurocritical Care
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: PHASE2
Enrollment: 88
Sponsor: Erasme University Hospital
Location: Erasme University Hospital Brussels
Summary
The LIMIT-TBI trial is a multicenter, international, randomized, phase II clinical trial designed to evaluate the feasibility and safety of targeting a neutral fluid balance compared to standard care in critically ill adult patients with traumatic brain injury (TBI).
Fluid therapy is a cornerstone of TBI management, but optimal fluid balance remains uncertain, with both fluid overload and restriction potentially leading to adverse outcomes. This study aims to determine whether maintaining a daily fluid balance close to zero (±500 mL) during the first 5 days of ICU admission is achievable and safe.
Participants will be randomized within 48 hours of ICU admission to either a protocolized neutral fluid balance strategy or standard care. Outcomes include feasibility of achieving the target balance, organ complications, hemodynamic parameters, ICU resource utilization, and mortality and neurological outcomes up to 6 months.
Eligibility Criteria
Inclusion Criteria:
* Adult patients with traumatic brain injury (isolated or associated with extracranial injuries), with or without intracranial pressure monitoring
* Admission to the intensive care unit
* Age \>18 years
* Enrollment within 48 hours after ICU admission
Exclusion Criteria:
* Enrollment in another clinical trial not approved for co-enrollment
* Pregnancy or suspected pregnancy
* Concomitant hemorrhagic shock expected to require surgical treatment within 24 hours from inclusion or requiring massive transfusion protocol
* Hemodynamic instability at ICU admission, defined as heart rate \>120 beats/min and systolic arterial pressure \0.5 mcg/kg/min) or any inotropic support
* Need for continuous venovenous hemodiafiltration (CVVHDF) at admission
* Expected survival \
Source: ClinicalTrials.gov (NCT07625995). StuddyBuddy aggregates publicly available trial information.