Actively Recruiting

Phase Not Applicable
Age: 18Years - 82Years
All Genders
Healthy Volunteers
NCT07357090

Carbon Dioxide Administration and Brain Waste Clearance

Led by Andrew Mayer · Updated on 2026-02-23

200

Participants Needed

1

Research Sites

304 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The current study tests whether different exposures to carbon dioxide (CO2) can safely result in the increased movement of proteins from the brain into the blood. The investigators believe that this would be a proxy for the brain clearing waste products more effectively. The current study will use a counter-balanced design, in which individuals with and without a history of traumatic brain injury (TBI) will receive different levels of CO2 (targeted changes of approximately 5 or 10 mmHG in end-tidal CO2) approximately one week apart. The counter-balanced design means that each participant receives a single dose of CO2 at each visit, and different doses of CO2 at each visit. The order in which participants receive the dose is randomized, and the participant will not be informed of the dose.

CONDITIONS

Official Title

Carbon Dioxide Administration and Brain Waste Clearance

Who Can Participate

Age: 18Years - 82Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Able to give valid informed consent
  • Aged 18 to 82 years
  • For TBI group: history of traumatic brain injury of any severity sustained at age 18 or older, confirmed by semi-structured interview
  • For healthy group: no history of TBI
Not Eligible

You will not qualify if you...

  • Contraindications to MRI scanning including pregnancy or claustrophobia
  • Unable to give valid informed consent or incarcerated
  • Diagnosed with Alzheimer's disease, ADRD, or mild cognitive impairment
  • History of autism spectrum disorder, intellectual disability, serious neurological conditions (e.g., epilepsy, tumors, neurosurgery) or psychiatric disorders requiring hospitalization prior to TBI onset (for TBI group)
  • Current or previous diagnosis of psychosis spectrum or bipolar disorder (for TBI group)
  • Respiratory diseases or pulmonary conditions increasing study risk (e.g., severe asthma, COPD)
  • History of cardiac arrhythmias
  • Current or past substance use disorder or regular substance use in past six months (healthy group)
  • Previous head injury with loss of consciousness over 30 minutes (healthy group)
  • Non-English fluency
  • Weigh under 110 pounds (blood draw requirement)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Mind Research Network

Albuquerque, New Mexico, United States, 87106

Actively Recruiting

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Research Team

J

Jody Roberts, MS

CONTACT

A

Andrew Mayer R The Mind Research Network, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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