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Hyperbaric Oxygen for Traumatic and Non-traumatic Brain Injury (HYBOBI2)

Primary Purpose

Brain Injury, Chronic

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Hyperbaric Oxygen
Minimal pressure air
Sponsored by
Lindell Weaver
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Injury, Chronic focused on measuring Concussion, Traumatic brain injury, Hyperbaric oxygenation, Post-concussion symptoms, Headache, Carbon monoxide

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults, age 18-70 years, both men and women
  • Able to speak and read English as primary language
  • Able and willing to provide written informed consent for study participation.
  • Able and willing to complete outcome assessments and provide blood and urine samples as required by the study protocol.
  • Able to tolerate the chamber environment and hood placement and to equalize middle ear pressure.
  • Past history of at least one brain injury with persistent symptoms that meets all of the following criteria:

    • Brain injury of non-stroke etiology that occurred at least 6 months but no more than 10 years prior to enrollment.
    • At least 3 of the following persistent symptoms from the injury: headaches, dizziness or balance problems, blurred vision, tiredness/fatigue or sleep problems, seizures, remembering things or solving problems, managing stress or emotional upsets, controlling temper/irritability, depression, anxiety, post-traumatic stress, or ringing in the ears.
  • Normal thyroid stimulating hormone and hematocrit value greater than 35% within the previous 6 months.

Exclusion Criteria:

  • Contraindications to hyperbaric oxygen

    • Insulin-dependent diabetes mellitus, or diabetes mellitus that is not reasonably controlled.
    • Uncontrolled seizure disorder (participants must be on therapy and seizure-free for at least 6 months).
    • Claustrophobia precluding chamber or hood tolerance.
    • Implanted devices not cleared for hyperbaric pressurization.
    • Pregnancy or plans to become pregnant during the study participation period. Women of childbearing potential will be asked to use an acceptable form of birth control during study participation.
    • Lung disease, such as emphysema, chronic bronchitis, asthma that is not well-controlled, or bullous lung disease that raises the risk for pulmonary barotrauma due to air trapping.
    • Active malignancy, previous malignancy (except basal cell carcinoma) in the last 5 years, or any prior treatment with bleomycin (Blenoxane). Prior treatment with doxorubicin (Adriamycin) is acceptable as long follow-up echocardiography is normal.
    • Chronic disease such as heart or renal failure would raise the participant's risk of adverse events during hyperbaric oxygen.
  • Confounds to the outcome assessments

    • Inability to speak English as their primary language (English fluency required because many of the outcomes are only in available in English)
    • Instability with walking requiring more than a cane for assistance
    • Alcohol abuse, by self-report, within the last year.
    • Lifetime history of illicit drug use, by self-report, except remote (greater than one year), non-habitual use of marijuana.
    • Failed urine drug screen during study participation.
    • Continued participation during the intervention period in sports activities where head injury is likely, such as contact football, boxing, mixed martial arts, etc.
    • Blind or deaf.
    • Major psychiatric disorder or degenerative mental disease (such as multiple sclerosis).
    • Prior therapeutic radiation to the central nervous system.
    • Personal history of any condition that pre-dates their brain injury that resulted in diminished capacity (such as chromosomal disorders) or that, in the opinion of the investigators, affects cognition to such a degree that the outcome assessments are invalidated (such as learning disability or attention deficit hyperactivity disorder requiring pharmaceutical therapy as an adult).
    • Any brain injury from stroke (ischemic or hemorrhagic)
    • Known untreated chronic or acute medical conditions, such as hypothyroidism, Cushing's disease, untreated hypertension, etc., that would confound the outcome assessments or inhibit compliance with the study protocol. If treated, these disorders would not be excluded.
    • Concomitant enrollment in any other drug/device clinical trial.
    • Prior hyperbaric oxygen for any reason within the last year.

Sites / Locations

  • Intermountain Medical Center
  • Intermountain LDS Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Hyperbaric Oxygen

Minimal pressure air

Arm Description

100% oxygen at 1.5 atmospheres absolute for 60 minutes, 40 sessions

Regular air at minimal pressurization for 60 minutes, 40 sessions

Outcomes

Primary Outcome Measures

Neurobehavioral Symptom Inventory
Participant-reported symptom rating of post-concussive symptoms

Secondary Outcome Measures

Neurobehavioral Symptom Inventory
Participant-reported symptom rating of post-concussive symptoms
Incidence of myopia
Myopic visual changes after chamber sessions

Full Information

First Posted
October 31, 2013
Last Updated
August 2, 2022
Sponsor
Lindell Weaver
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1. Study Identification

Unique Protocol Identification Number
NCT01986205
Brief Title
Hyperbaric Oxygen for Traumatic and Non-traumatic Brain Injury
Acronym
HYBOBI2
Official Title
A Double-blind Randomized Trial of Hyperbaric Oxygen Versus Sham for Persistent Symptoms After Brain Injury
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
September 6, 2017 (Actual)
Primary Completion Date
May 31, 2022 (Actual)
Study Completion Date
May 31, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Lindell Weaver

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to examine whether 40 hyperbaric oxygen sessions has effect on long-term symptoms after brain injury. This study will enroll 90 individuals with persistent problems 6 months to 10 years after a brain injury. These individuals will be randomized to receive either oxygen or air in a pressurized hyperbaric chamber. Participants will receive 40 daily hyperbaric chamber sessions. Participants will have a series of tests and questionnaires before they begin their chamber sessions, after they complete 40 sessions, and 6 months after they joined the study. These tests include computer-based and pencil-and-paper questionnaires and thinking tests, brain imaging, a neurological examination, and an eye exam. Participants will also be asked to provide blood for future research. After the 6-month tests are complete, all participants will receive 40 hyperbaric oxygen sessions, then undergo the same tests at 9 months and 12 months.
Detailed Description
This is a single center, randomized, double-blind study with a subsequent open-label intervention period to explore whether a course of hyperbaric oxygen can ameliorate persistent symptoms after brain injury. In this study, adult men and women with persistent symptoms 6 months to 10 years after injury will be randomized to receive 40 hyperbaric oxygen sessions (100% oxygen at 1.5 atmospheres absolute, 60 minutes door-to-door) or sham chamber sessions (room air chamber excursion at near-ambient pressure, 60 minutes door-to-door). Chamber sessions will be provided Monday through Friday, excluding holidays, and participants will have up to 12 weeks to complete their 40 sessions. Participants will be evaluated before the chamber sessions, at 13 weeks, and at 6 months. Assessments include self-administered questionnaires, neuropsychological function, a brief neurological examination, electroencephalography, visual function tests, and a neuro-optometry evaluation. These outcome tools will measure symptoms and deficit at the time of enrollment and subsequent evaluations, and provide insight into whether hyperbaric oxygen can play a role in recovery from brain injury. Once the participants have completed their 6 month evaluations, they will enter an open intervention group, receiving 40 hyperbaric sessions at 1.5 atmospheres absolute for 60 minutes. Participants will have up to 12 weeks to complete these sessions. Participants will be evaluated after the second set of chamber sessions (at 9 months and again at 12 months). Individuals will then be assessed annually until study closure (12-month follow-up of the last enrolled participant). Participants will be asked to provide blood for long-term storage of serum, plasma, and DNA for future investigations, including apolipoprotein E genotype.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Injury, Chronic
Keywords
Concussion, Traumatic brain injury, Hyperbaric oxygenation, Post-concussion symptoms, Headache, Carbon monoxide

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
49 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Hyperbaric Oxygen
Arm Type
Experimental
Arm Description
100% oxygen at 1.5 atmospheres absolute for 60 minutes, 40 sessions
Arm Title
Minimal pressure air
Arm Type
Placebo Comparator
Arm Description
Regular air at minimal pressurization for 60 minutes, 40 sessions
Intervention Type
Combination Product
Intervention Name(s)
Hyperbaric Oxygen
Other Intervention Name(s)
HBO2, HBOT, HBO, Hyperbaric oxygen therapy
Intervention Description
Hyperbaric oxygen (USP oxygen >99%) delivered in a hyperbaric chamber pressurized to 1.5 atmospheres absolute.
Intervention Type
Combination Product
Intervention Name(s)
Minimal pressure air
Other Intervention Name(s)
Room air
Intervention Description
Room air delivered in a hyperbaric chamber with minimal pressurization.
Primary Outcome Measure Information:
Title
Neurobehavioral Symptom Inventory
Description
Participant-reported symptom rating of post-concussive symptoms
Time Frame
13 weeks
Secondary Outcome Measure Information:
Title
Neurobehavioral Symptom Inventory
Description
Participant-reported symptom rating of post-concussive symptoms
Time Frame
6 months
Title
Incidence of myopia
Description
Myopic visual changes after chamber sessions
Time Frame
13 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults, age 18-70 years, both men and women Able to speak and read English as primary language Able and willing to provide written informed consent for study participation. Able and willing to complete outcome assessments and provide blood and urine samples as required by the study protocol. Able to tolerate the chamber environment and hood placement and to equalize middle ear pressure. Past history of at least one brain injury with persistent symptoms that meets all of the following criteria: Brain injury of non-stroke etiology that occurred at least 6 months but no more than 10 years prior to enrollment. At least 3 of the following persistent symptoms from the injury: headaches, dizziness or balance problems, blurred vision, tiredness/fatigue or sleep problems, seizures, remembering things or solving problems, managing stress or emotional upsets, controlling temper/irritability, depression, anxiety, post-traumatic stress, or ringing in the ears. Normal thyroid stimulating hormone and hematocrit value greater than 35% within the previous 6 months. Exclusion Criteria: Contraindications to hyperbaric oxygen Insulin-dependent diabetes mellitus, or diabetes mellitus that is not reasonably controlled. Uncontrolled seizure disorder (participants must be on therapy and seizure-free for at least 6 months). Claustrophobia precluding chamber or hood tolerance. Implanted devices not cleared for hyperbaric pressurization. Pregnancy or plans to become pregnant during the study participation period. Women of childbearing potential will be asked to use an acceptable form of birth control during study participation. Lung disease, such as emphysema, chronic bronchitis, asthma that is not well-controlled, or bullous lung disease that raises the risk for pulmonary barotrauma due to air trapping. Active malignancy, previous malignancy (except basal cell carcinoma) in the last 5 years, or any prior treatment with bleomycin (Blenoxane). Prior treatment with doxorubicin (Adriamycin) is acceptable as long follow-up echocardiography is normal. Chronic disease such as heart or renal failure would raise the participant's risk of adverse events during hyperbaric oxygen. Confounds to the outcome assessments Inability to speak English as their primary language (English fluency required because many of the outcomes are only in available in English) Instability with walking requiring more than a cane for assistance Alcohol abuse, by self-report, within the last year. Lifetime history of illicit drug use, by self-report, except remote (greater than one year), non-habitual use of marijuana. Failed urine drug screen during study participation. Continued participation during the intervention period in sports activities where head injury is likely, such as contact football, boxing, mixed martial arts, etc. Blind or deaf. Major psychiatric disorder or degenerative mental disease (such as multiple sclerosis). Prior therapeutic radiation to the central nervous system. Personal history of any condition that pre-dates their brain injury that resulted in diminished capacity (such as chromosomal disorders) or that, in the opinion of the investigators, affects cognition to such a degree that the outcome assessments are invalidated (such as learning disability or attention deficit hyperactivity disorder requiring pharmaceutical therapy as an adult). Any brain injury from stroke (ischemic or hemorrhagic) Known untreated chronic or acute medical conditions, such as hypothyroidism, Cushing's disease, untreated hypertension, etc., that would confound the outcome assessments or inhibit compliance with the study protocol. If treated, these disorders would not be excluded. Concomitant enrollment in any other drug/device clinical trial. Prior hyperbaric oxygen for any reason within the last year.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lindell K. Weaver, MD
Organizational Affiliation
Intermountain Health Care, Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Intermountain Medical Center
City
Murray
State/Province
Utah
ZIP/Postal Code
84157
Country
United States
Facility Name
Intermountain LDS Hospital
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84143
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
23682548
Citation
Churchill S, Weaver LK, Deru K, Russo AA, Handrahan D, Orrison WW Jr, Foley JF, Elwell HA. A prospective trial of hyperbaric oxygen for chronic sequelae after brain injury (HYBOBI). Undersea Hyperb Med. 2013 Mar-Apr;40(2):165-93.
Results Reference
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Hyperbaric Oxygen for Traumatic and Non-traumatic Brain Injury

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