Study Stopped
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Hyperbaric Oxygenation (HBO) in Traumatic Spinal Cord Injury. (EOS) - Pilot Study
1 other identifier
interventional
11
1 country
1
Brief Summary
Hypothesis of the Study: Based on the presented results, the investigator hypothesises that HBO preserves neurons that are not irreversibly damaged (i.e. severed) during initial trauma, thus enabling regain of their function. The investigator predicts that HBO treatment protects and enhances motor function in initially paralysed regions, including improvement in function of the extremities as well as recovery of urinary bladder control and bowel function. Outline of the Proposed Study: Within a prospective "proof of principle" trial, a total of 100 patients will be included. Fifty patients will be recruited at the Division of Thoracic and Hyperbaric Surgery, Medical University of Graz. In parallel, 50 control patients will be included at the Department of Orthopaedics and Trauma, Paracelsus University Salzburg, Salzburger Landeskliniken (SALK), Austria. Thereby, all patients that are admitted at the Medical University of Graz can be treated and the enrolment of 50 patients into the treatment group can be implemented within the outlined time frame. The active recruitment period is planned for three years. Both HBO treated and control patients will undergo the same surgical and nonsurgical procedures. HBO treatment will be started within 24 hours after the injury. A total of 21 consecutive daily sessions will be applied, followed by routine rehabilitation programmes. By matching control and HBO-treated patients, an evaluation of the treatment effect of HBO is possible. The outcome will be evaluated by implementing the American Spinal Injury Association (ASIA)-scores and magnet resonance (MR) imaging. Additionally, inflammatory and regenerative blood markers will be analysed (neuroendocrine markers/neuro-transmitters: S100beta, Brain Derived Neurotrophic Growth Factor \[BDNF\], Glial Fibrillary Acidic Protein \[GFAP\], Reactive Oxygen Species (ROS), norepinephrine; array of pro- and anti-inflammatory cytokines and chemokines).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_2
Started Apr 2017
Longer than P75 for phase_2
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 22, 2017
CompletedFirst Posted
Study publicly available on registry
April 5, 2017
CompletedStudy Start
First participant enrolled
April 18, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 20, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 20, 2024
CompletedMay 9, 2025
March 1, 2023
7.7 years
March 22, 2017
May 6, 2025
Conditions
Outcome Measures
Primary Outcomes (2)
Improvement of neurological deficits caused by spinal cord lesions
assessed by American Spinal Injury Association (ASIA) scores
Change from baseline-admission scores ( ASIA ) at 12 months
Correlation of clinical observations with blood parameters
assessed by routinely taken blood tests
Blood samples will be taken at the time of admission, immediately before the first HBO, immediately after the first HBO, on days 1, 3, 7, 14 , 21 before the respective HBO, and at the 35 days and two months follow-up
Study Arms (2)
test
ACTIVE COMPARATORHBO, ASIA score, blood taking
control
NO INTERVENTIONASIA score, blood taking
Interventions
Hyperbaric oxygenation (HBO) is defined as breathing of 100% oxygen under elevated ambient pressure in a hyperbaric chamber. HBO is considered a pharmacological therapy.
Eligibility Criteria
You may qualify if:
- Test cohort and control cohort:
- age: 16 to 70 years
- Traumatic spinal cord injury
- Initial incomplete or complete (ASIA) sensor/motoric dysfunction
- Mentally competent patient (no mental disability in history in case of intubated patient)
- No relevant neuromuscular diseases / neurological deficits before trauma
- Vertebral column stable, no relevant mechanical compression of spinal cord with our without surgical intervention within 24 hours after the injury;
- Spinal MRI and CT-scan within first 24 hours
- Test cohort only:
- Cardiorespiratory situation allowing safe application of HBO
- Ability to equalize pressure differences in middle ear confirmed by an ENT (ear, nose, throat) physician or pretherapeutic myringotomy
- Circumstances allowing HBO-treatment to be started \< 24 hours after the injury
You may not qualify if:
- Test cohort and control cohort:
- Morphologically confirmed complete discontinuation of the spinal cord
- Cardio-respiratory instability
- Persistent seizure activity in spite of medication
- Craniocerebral injury exceeding mere commotion
- Pregnancy
- Sepsis, Systemic Inflammatory Response Syndrome (SIRS)
- Simultaneous participation in another interventional study if relevant
- Test cohort only:
- Cystic or bullous lung disease, untreated pneumothorax
- Treatment with doxorubicin in patient´s history
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Medical University Graz
Graz, Austria
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 22, 2017
First Posted
April 5, 2017
Study Start
April 18, 2017
Primary Completion
December 20, 2024
Study Completion
December 20, 2024
Last Updated
May 9, 2025
Record last verified: 2023-03