Actively Recruiting

Phase 4
Age: 18Years - 75Years
All Genders
NCT07426458

Ventilation and Perfusion in Asthmatics

Led by University of Miami · Updated on 2026-05-05

40

Participants Needed

1

Research Sites

100 weeks

Total Duration

On this page

Sponsors

U

University of Miami

Lead Sponsor

A

Australian Lung Health Initiative Pty Ltd

Collaborating Sponsor

AI-Summary

What this Trial Is About

Assess regional changes to perfusion and ventilation from inhaled corticosteroid (ICS) and Fast-acting beta-antagonist (FABA) among adult asthmatics using radiographically derived estimates of regional ventilation (V-distribution), ventilation defect percentage (VDP), and ventilation heterogeneity (VH).

CONDITIONS

Official Title

Ventilation and Perfusion in Asthmatics

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Physician diagnosis of asthma
  • Baseline Forced Expiratory Volume in 1 Second (FEV1) < 80% of predicted with at least 10% reversibility after bronchodilator
  • Adults between 18 and 75 years old
  • Using a stable dose of inhaled corticosteroids for at least 3 months before enrollment
Not Eligible

You will not qualify if you...

  • Current cigarette smoking or history of more than 10 pack-years
  • Current use of nicotine vaping
  • Pregnant or breastfeeding women
  • Respiratory infection within 4 weeks before study
  • Forced Expiratory Volume in 1 Second (FEV1) less than 50%
  • Intolerance to inhaled corticosteroids or fast-acting beta agonists
  • Use of beta-blocker medications
  • Use of systemic glucocorticosteroids or oral methyl-xanthines within 30 days before study visit

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

University of Miami - Converge Miami

Miami, Florida, United States, 33136

Actively Recruiting

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Research Team

M

Maria McCoy

CONTACT

S

Sonia Dipti Meena Velmurugan, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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