Microglia Activation in Asthma

Status: Recruiting
Location: See location...
Intervention Type: Radiation, Biological
Study Type: Observational
SUMMARY

The goal of this clinical trail is to learn about how asthma influences brain function. The main questions it aims to answer are: * How airway inflammation in asthma affects the brain; and, * Whether airway inflammation in asthma is related to symptoms of depression and anxiety Over the course of 6 visits, participants will: * Complete questionnaires * Complete computer tasks * Undergo allergy skin test * Undergo breathing tests including two whole lung allergen challenges * Give four blood samples * Complete brain imaging scans

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Individuals with no health concerns that might affect the outcome of the study.

• Age 18-75 years of age.

• Physician diagnosis of asthma for at least six months prior to screening (can be determined at the discretion of an asthma/allergy physician member of the study team). Mild asthma will be defined as asthma that is well controlled with low-intensity treatment, e.g., SABA alone, as-needed low-dose ICS-LABA, or low-dose ICS plus as-needed SABA.

• At least a 20% decrease in forced expiratory volume (FEV1) during the immediate response following the screening inhaled allergen challenge.

• FEV1 ≥ 70% predicted at baseline.

• Positive immediate skin test for allergies to cat hair, house dust mite, or ragweed (historical data documented within the last 5 years with our research group is acceptable).

• Ability to tolerate a simulated MRI brain scanning session.

• In the opinion of the investigator, capable and willing to grant written informed consent and cooperate with study procedures and requirements.

• High-affinity TSPO-binding genotype. Mixed (high/low) binding-affinity genotype may be included at PIs discretion.

Locations
United States
Wisconsin
University of Wisconsin Madison
RECRUITING
Madison
Contact Information
Primary
Rachel Kaspari
maia@medicine.wisc.edu
608-263-0524
Backup
Danika Klaus
maia@medicine.wisc.edu
608-263-0524
Time Frame
Start Date: 2019-12-17
Estimated Completion Date: 2028-08-01
Participants
Target number of participants: 50
Related Therapeutic Areas
Sponsors
Leads: University of Wisconsin, Madison
Collaborators: National Institute on Aging (NIA), National Heart, Lung, and Blood Institute (NHLBI)

This content was sourced from clinicaltrials.gov