Recruiting

Observational Study

Sponsor:

University of Wisconsin, Madison

Code:

NCT06299592

Conditions

Asthma

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Accepted

Interventions

PET/MRI using [18F]FEPPA tracer

Study Details

Brief summary:

The goal of this clinical trial 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 3 visits, participants will:

  • Complete questionnaires
  • Complete computer tasks
  • Undergo allergy skin test and breathing tests
  • Give two blood samples
  • Give a sputum sample
  • Complete brain imaging scans

Researchers will compare results between participants with asthma, and participants who do not have asthma.

Conditions

Asthma

Study ID

NCT06299592

Start date

Mar 6, 2024

Status verified date

May, 2026

Completion date

Aug, 2028

Anticipated

Primary completion date

Aug, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • Ability to understand and the willingness to sign a written informed consent document
  • Individuals with no health concerns that might affect the outcome of the study
  • Age 18-75 years of age
  • 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
  • For participants with severe asthma:

  • 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)
  • Severe asthmatics must meet the ATS definition of severe asthma and/or be currently receiving a GINA Step 4 or 5 therapy or daily treatment of 320mcg budesonide. Therapy may include ongoing use of currently approved biologic immunomodulators

Exclusion Criteria:

  • Current smoker (defined as more than 0.5 pack per week for the past 6 months and any smoking within two weeks of study procedures) or has a smoking history exceeding 5 pack years within the last 10 years
  • Currently receiving allergen immunotherapy unless on stable dose.
  • Use of psychotropic medication that might affect function of neurocircuitry implicated in our hypotheses (at the discretion of the PI/Co-I)
  • Inability to hold medications detailed in the medication hold schedule
  • Needle phobia or claustrophobia
  • Major health problems such any of the following in the last 6 months: stroke/TIA, myocardial Infarction, stent placement, or acute coronary syndrome are definitively exclusionary. Decisions regarding other major health problems, such as autoimmune disease, history of carotid stenosis, heart disease, uncontrolled hypertension, lung diseases other than asthma, history of significant arrhythmias, etc. will be based upon the judgement of the PI/Co-I.
  • Use of biologic medication that might affect signaling pathways under investigation (at the discretion of the PI/Co-I)
  • Pre-existing chronic infectious disease
  • Scheduled use of non-selective beta-blockers prior to each study visit.
  • Use of an investigational drug within 30 days of entering the study. This criterion will be reviewed on a case by case basis by the PI/Co-I to determine appropriate washout period. Appropriate wash out period may be greater than 30 days depending on the half-life of the investigational drug. Participants may be eligible for study participation after completing the washout period designated by the PI or Co-I (physician only).
  • Any MRI incompatibility as determined by most current MRI screening form
  • History of a diagnosed bipolar disorder, schizophrenia, or schizoaffective disorder
  • History of serious head trauma or seizure disorder (can be included at the discretion of the PI or Co-I)
  • Unable, in the judgement of the investigator, to comply with directions and/or tolerate the procedures required for participation in this study
  • Pregnant or breast-feeding or has a planned pregnancy during the course of the study
  • Any other medical condition or disease that would impact participant safety or data integrity in the opinion of the PI/CO-I

Study Design

Enrollment

100 participants

Anticipated

Interventions and Outcome Measures

Arms

Participants with asthma

Participants without asthma

Interventions

PET/MRI using [18F]FEPPA tracer

PET/MRI scans with \[18F\]FEPPA radiotracer selective for translocator protein (TSPO) binding, which is elevated in activated microglia

Primary outcome measure

  • Binding of [18F]-FEPPA [ Time Frame: Up to 2 weeks ]

Central Contacts and Locations

Central contacts

Rachel Kaspari

608-263-0524maia@medicine.wisc.edu

Danika Klaus

608-263-0524maia@medicine.wisc.edu

Locations

Center for Healthy Minds

Recruiting

Madison, Wisconsin, United States, 53703

Contacts

Janelle Grogan

608-263-0524jegrogan@medicine.wisc.edu

Principal Investigator:

Melissa Rosenkranz, PhD

More Information

Sponsor

University of Wisconsin, Madison

Last update posted

Aug 5, 2026

Last verified

May, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-05. This information was provided to ClinicalTrials.gov by University of Wisconsin, Madison on 2026-08-05.