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Enrolling by invitation NCT04258774

The Effect of Respiratory Challenge on the BOLD Signal

No phase Interventional Hypoxia, Brain Hyperoxia Hypercapnia Hypocapnia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Carbon Dioxide.
Who it may be relevant to
Registry conditions: Hypoxia, Brain, Hyperoxia, Hypercapnia, Hypocapnia. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Overview

The purpose of this research study is to better understand how blood flow and metabolism are different between normal controls and patients with disease. The investigators will examine brain blood flow and metabolism using magnetic resonance imaging (MRI). The brain's blood vessels expand and constrict to regulate blood flow based on the brain's needs. The amount of expanding and contracting the blood vessels can do varies by age. The brain's blood flow changes in small ways during everyday activities, such as normal brain growth, exercise, or deep concentration. Significant illness or physiologic stress may increase the brain's metabolic demand or cause other bigger changes in blood flow. If blood vessels are not able to expand to give more blood flow when metabolic demand is high, the brain may not get all of the oxygen it needs. In less extreme circumstances, not having as much oxygen as it wants may cause the brain to grow and develop more slowly than it should. One way to test the ability of the blood vessels to expand is by measuring blood flow while breathing in carbon dioxide (CO2). CO2 causes blood vessels in the brain to dilate without increasing brain metabolism. The study team will use a special mask to control the amount of oxygen and carbon dioxide patients breath in so that we can study how their brain reacts to these changes. This device designed to simulate carbon dioxide levels achieved by a breath-hold and target the concentration of carbon dioxide in the blood in breathing patients. The device captures exhaled gas and provides an admixture of fresh gas and neutral/expired gas to target different carbon dioxide levels while maintaining a fixed oxygen level. The study team will obtain MRI images of the brain while the subjects are breathing air controlled by the device.

Interventions

  • Other Carbon Dioxide
    The study team will administer inhaled carbon dioxide to the participants during an MRI at a level

Primary outcome measures

  • Cerebral Oxygen Metabolism [Time frame: From the beginning of the MRI scan to the completion of the MRI scan -- 75 minutes.]
Secondary outcome measures (1)
  • Cerebrovascular Reactivity [Time frame: From administration of carbon dioxide to end of inhalation of carbon dioxide -- 15 minutes.]

Eligibility criteria

Inclusion criteria

  • Healthy adult subjects (>18 years old) OR adult patients (>18 years old) diagnosed with vascular pathology of the brain willing to participate and sign a consent form.
  • Able to participate in MRI scan without sedation
  • Not on stimulant medications
  • No psychiatric history, as defined by seeing a psychiatrist for medical evaluation and treatment, or taking anti-depressant medications
  • No seizure history
  • May have occasional headaches if not taking a daily preventative medication for headaches
  • Not on vasodilatory medication, such as sildenafil or verapamil

Exclusion criteria

  • Subjects refusing to undergo testing
  • Subjects with obstructive or resistive lung disease whose PaCO2 at rest is greater than 50mmHg or whose venous serum bicarbonate is greater than 26 mEq/L
  • Subjects with pre-existing respiratory or metabolic acidosis
  • Subjects who require portable oxygen at rest or with exercise
  • Subjects with chronic heart failure or severe pulmonary disease who are unable to climb one flight of stairs due to shortness of breath
  • Subjects with severe heart failure or restrictive lung disease with resting respiratory rate over 15 breaths/min 2. Patients that cannot participate in a course of rehabilitation therapy.
  • Subjects that cannot undergo an MRI scan due to one of the following indications:
  • Pregnancy
  • Obtundation, or Coma
  • Confusion, Delirium, or Dementia
  • Unable to understand or carry out commands regarding keeping still and breathing pattern
  • Increased intracranial pressure due to space occupying lesion or obstruction of outflow of CSF
  • Claustrophobia
  • History of kidney problems
  • Pace makers
  • Skin tattoos
  • Neurostimulators (TENS-unit)
  • Implanted drug infusion device (i.e., insulin pump)
  • Exposure of metal fragments to your eye
  • Artificial heart valves
  • Aneurysm clips
  • Cochlear implants
  • Metallic implants and prosthesis
  • Vascular stent or stent graft
  • History as a metal worker
  • Shrapnel or bullet wounds
  • Dorsal column stimulators

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

United States · 1 center
  • Washington University of St. Louis — St Louis

Identifiers

NCT: NCT04258774 · 201910105

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗