Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02577497 · ClinicalTrials.gov registry record · Phase 4

Effect of Extra- Fine Versus Coarse-Particle Inhaled Corticosteroids (ICS) on Ventilation Heterogeneity in Children With Poorly Controlled Asthma

A Phase 4 study of Asthma, sponsored by University of Virginia.

Completed
Registry status
Phase 4
Development phase
31
Enrollment target
1
Study location

NCT02577497: Completed Phase 4 study of Asthma, sponsored by University of Virginia.

NCT02577497 is a Phase 4 study of Asthma that has completed, run by University of Virginia. The registered enrollment target is 31 participants, below the 1,563-participant average among 374 other Asthma trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02577497, a Phase 4 study of Asthma, has completed, sponsored by University of Virginia.

COMPLETED
Registry status
Phase 4
Development phase
31 participants
Enrollment target
1
Study location

Study Summary

The primary objective of the study is to show that ventilation heterogeneity identified by hyperpolarized helium-3 lung MRI is prevalent children with poorly controlled asthma despite guidelines-based treatment with ICS. The secondary objective is to demonstrate whether or not eight weeks of treatment with extra-fine particle ICS (HFA-BDP) improves ventilation heterogeneity compared to treatment with a coarse particle ICS (fluticasone HFA or dry powder).

Primary Outcome

VHI = lung defect volume divided by total lung volume. It is a ratio scale.

Conditions Studied

Interventions

  • DRUG beclomethasone
  • DRUG fluticasone

Study Locations (1)

Virginia

  • University of Virginia - Fontaine Research Park - Charlottesville

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2016-06
Est. Completion 2018-07-06
Phase Phase 4
University of Virginia

449 total trials

What the finished NCT02577497 record still lists

NCT02577497 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 1,563-participant average among 374 other Asthma trials with a reported enrollment target (98% lower).

The record links to 1 condition, with Asthma appearing as the primary indexed condition, and to 2 interventions - of which beclomethasone is the first listed.

NCT02577497 reports a single indexed study location in Virginia.

Frequently Asked Questions

What is clinical trial NCT02577497 about?

NCT02577497 is a clinical study titled "Effect of Extra- Fine Versus Coarse-Particle Inhaled Corticosteroids (ICS) on Ventilation Heterogeneity in Children With Poorly Controlled Asthma". The primary objective of the study is to show that ventilation heterogeneity identified by hyperpolarized helium-3 lung MRI is prevalent children with poorly controlled asthma despite guidelines-based treatment with ICS. The secondary objective is to demonstrate whether or not eight weeks of treatme...

What is the current status of trial NCT02577497?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 31 participants. The study started on 2016-06. Estimated completion is 2018-07-06.

What conditions does trial NCT02577497 study?

This clinical trial studies the following conditions: Asthma.

What interventions are being tested in trial NCT02577497?

The interventions under investigation include: beclomethasone (DRUG), fluticasone (DRUG).

Who is sponsoring clinical trial NCT02577497?

This trial is sponsored by University of Virginia, which has 449 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02577497 being conducted?

This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Asthma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02577497's enrollment target sits among peer trials

31 301st of 374 higher than 71 of 374 other Asthma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Asthma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02932618 · 31 participants · Phase 3

    A Study of Recombinant Von Willebrand Factor (rVWF) With or Without ADVATE in Children With Severe Von Willebrand Disease (VWD)

  • NCT03482297 · 31 participants · Phase 1

    Automated Abdominal Binder for Orthostatic Hypotension

  • NCT04016389 · 31 participants · NA

    FIGO 2018 Stage IB2 Cervical Cancer Treated With Neoadjuvant Chemotherapy Followed by Fertility Sparing Surgery

  • NCT04211675 · 31 participants · Phase 1

    NK Cells Infusions With Irinotecan, Temozolomide, and Dinutuximab

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02577497, the US trial registry maintained by the National Library of Medicine. NCT02577497 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.