Loading clinical trials...
Loading clinical trials...
Hyperbaric Oxygen Brain Injury Treatment (HOBIT) Trial
The purpose of this innovative adaptive phase II trial design is to determine the optimal combination of hyperbaric oxygen treatment parameters that is most likely to demonstrate improvement in the outcome of severe TBI patients in a subsequent phase III trial.
Preclinical and clinical investigations strongly indicate that hyperbaric oxygen (HBO2) is physiologically active in improving the destructive processes in severe Traumatic Brain Injury (TBI). However, prior to a definitive efficacy study, important information is required regarding optimizing the HBO2 treatment paradigm instituted in terms of pressure and whether NBH enhances the clinical effectiveness of the HBO2 treatment. Preclinical investigators working with TBI models have used pressures varying from 1.5 to 3.0 atmospheres absolute (ATA). Clinical investigators have used pressure varying from 1.5 to 2.5 ATA. However, the lungs in severe TBI patients have frequently been compromised by direct lung injury and/or acquired ventilator pneumonia and are susceptible to oxygen (O2) toxicity. Working within these constraints, it is essential to determine the most effective HBO2 treatment parameters without producing O2 toxicity and clinical complications. This proposed clinical trial is designed to answer these questions and to provide important data to plan a definitive efficacy trial.
Age
16 - 65 years
Sex
ALL
Healthy Volunteers
No
UCSD Medical Center - Hillcrest Hospital
San Diego, California, United States
St. Mary's Medical Center
West Palm Beach, Florida, United States
University of Iowa Hospitals and Clinics
Iowa City, Iowa, United States
University of Kentucky Hospital
Lexington, Kentucky, United States
University of Maryland
Baltimore, Maryland, United States
Detroit Receiving Hospital
Detroit, Michigan, United States
Hennepin County Hospital
Minneapolis, Minnesota, United States
University of Nebraska Medical Center
Omaha, Nebraska, United States
Duke University Hospital
Durham, North Carolina, United States
The Ohio State University Wexner Medical Center
Columbus, Ohio, United States
Start Date
June 25, 2018
Primary Completion Date
October 26, 2028
Completion Date
June 30, 2029
Last Updated
October 3, 2025
200
ESTIMATED participants
Hyperbaric oxygen (1.5 ATA, no NBH)
DRUG
Hyperbaric oxygen (2.0 ATA, no NBH)
DRUG
Hyperbaric oxygen (2.5 ATA, no NBH)
DRUG
Hyperbaric oxygen (1.5 ATA + NBH)
DRUG
Hyperbaric oxygen (2.0 ATA + NBH)
DRUG
Hyperbaric oxygen (2.5 ATA + NBH)
DRUG
Normobaric Hyperoxia (NBH)
DRUG
Usual Care
OTHER
Lead Sponsor
Gaylan Rockswold
Collaborators
NCT04521881
NCT07455136
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06725108