Concussion Clinical Trial
Official title:
Q-collar and Brain Injury Biomarkers
NCT number | NCT02271451 |
Other study ID # | 2014-5009 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 2014 |
Est. completion date | October 2015 |
Verified date | August 2020 |
Source | Children's Hospital Medical Center, Cincinnati |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Significant morbidity, mortality, and related costs are caused by traumatic brain injury
(TBI). A simple, effective, and lightweight device worn by athletes or war fighters in the
field, designed to mitigate TBI resulting from blast trauma or concussive events, would save
lives, and the huge costs currently being experienced for life-treatment of surviving
victims. An externally-worn medical device that applies mild jugular compression according to
the principle of the Queckenstedt Maneuver (the Device) is being developed by Q30 Labs, LLC
(Q30). Initial research suggests that the Device has the potential to reduce the likelihood
of TBI. The currently developed collar (Smith 2009; Smith 2011; Smith 2011; Smith 2012) has
been approved for studies in humans and the results indicate safety for use during high
demand and maximal exertion activities, Study ID: 2013-2240, Institutional Review Board -
Federalwide Assurance #00002988). Regarding safety, the externally worn collar is
meticulously designed to mimic the body's own omohyoid muscle actions upon the jugular veins
that will provide similar pressure and volume increases not to surpass that of a yawn or the
mere act of just lying down.
This study will investigate the effectiveness of this device in high school athletes playing
a collision or contact sport such as football, hockey, or lacrosse. The high risk sports
which utilize helmets during competition will allow for measurements systems to be embedded
in the headgear and will not affect play or fit of equipment. Athletes participating in this
study will be enrolled into one of two groups 1) device wearing or 2) non-device wearing. By
the nature of the sports selected, it is likely this pilot study will primarily include
males, however if any female meets inclusion criteria on the team selected they will be
included in this pilot investigation. The helmets of all participants will be outfitted with
an accelerometer which will measure the magnitude of every impact to the head sustained by
the athlete. Effectiveness of the device will be determined by brain imaging during the
pre-season, midseason, and end of season time points. A subset of athletes who report a
diagnosed concussion will also receive additional brain imaging within the week following the
diagnosed concussive event.
Status | Completed |
Enrollment | 15 |
Est. completion date | October 2015 |
Est. primary completion date | May 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 14 Years to 19 Years |
Eligibility |
Inclusion Criteria: - • Normal healthy volunteer - Able to provide written consent - Must be 14 years or older and a participant on a competitive and organized sports program - Neck circumference of 15 ½ - 16 ½ inches Exclusion Criteria: - • Unable to provide written consent - History of neurological deficits, previous cerebral infarction, or severe head trauma - Medical contraindications to restriction of venous outflow via the internal jugular veins (known increased intracerebral pressure, metabolic acidosis or alkalosis) - Glaucoma (Narrow Angle or Normal Tension) - Hydrocephalus - Recent penetrating brain trauma (within 6 months) - Known carotid hypersensitivity - Known increased intracranial pressure - Central vein thrombosis - Any known airway obstruction - Any known seizure disorder |
Country | Name | City | State |
---|---|---|---|
United States | Cincinnati Children's Hospital | Cincinnati | Ohio |
Lead Sponsor | Collaborator |
---|---|
Children's Hospital Medical Center, Cincinnati |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Longitudinal DTI Changes | measured white matter changes, mean diffusivity (MD), and radial diffusivity (RD) | 2 years |
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