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Study identifier: NCT05889650 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

External Lumbar Drainage to Reduce ICP in Severe TBI: a Phase 1 Clinical Trial

Condition: Severe Traumatic Brain Injury · Intracranial Hypertension  ·  Sponsor: Brain Trauma Foundation

PhaseNA
Planned participants30
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

The goal of this phase 1 randomized controlled safety and feasibility clinical trial are to determine the safety of external lumbar drainage (ELD) in select patients with severe Traumatic Brain Injury (TBI). The main questions it aims to answer are (i) if ELD is feasible and (ii) safe to perform in severe TBI patients who have radiological evidence of patent basal cisterns and midline shift \<5mm without increasing the risk of neurological worsening or cerebral herniation. All participants will receive routine usual care. The study group will additionally have ELD for cerebrospinal fluid (CSF) drainage. A comparison will be made between the usual treatment plus ELD (interventional) groups, and the usual treatment (control) groups on incidence rate of neurological worsening or cerebral herniation events, and whether total hours with raised intracranial pressure (ICP) are different.

This description comes directly from the study's public registry record.

Talk to the study team

Carlos Morales, MPH  ·  240-6536638  ·  carlos.morales.ctr@usuhs.edu

Halinder S Mangat, MD, MSc  ·  913-5886970  ·  elastic@braintrauma.org

Always discuss trial participation with your own doctor first.

Locations (6)

University of FloridaGainesville, Florida, United StatesRecruiting
Kansas University Medical CenterKansas City, Kansas, United StatesRecruiting
University of Texas Southwestern Medical CenterDallas, Texas, United StatesRecruiting
Brooke Army Medical CenterFort Sam Houston, Texas, United StatesRecruiting
University of Houston Medical CenterHouston, Texas, United StatesRecruiting
University of TexasSan Antonio, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05889650