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NCT04002362 · ClinicalTrials.gov registry record · Phase 2

Symptom Clusters in Children With Exacerbation-prone Asthma

A Phase 2 study, sponsored by Emory University.

Completed
Registry status
Phase 2
Development phase
68
Enrollment target

NCT04002362: Completed Phase 2 study, sponsored by Emory University.

NCT04002362 is a Phase 2 study that has completed, run by Emory University. The registered enrollment target is 68 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (49% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04002362, a Phase 2 study, has completed, sponsored by Emory University.

COMPLETED
Registry status
Phase 2
Development phase
68 participants
Enrollment target

Study Summary

Pediatric participants with exacerbation-prone asthma will receive an intramuscular injection of triamcinolone acetonide and will be followed for 48 weeks. The study visit 2 weeks after the injection will assess the response to the study medication, while the remaining study visits will examine the temporal stability of the symptom clusters.

Primary Outcome

Responsiveness to the study treatment is assessed with the Asthma Control Questionnaire (ACQ). This 7-item questionnaire includes questions related to daytime and nocturnal symptoms, short-acting bronchodilator use, and lung function during the clinic visit on that day. Participants report how difficult their asthma was to control on a scale from 0 (no impairment) to 6 (maximum impairment). Total raw scores range from 0 to 42, with higher scores indicating poorer asthma control. Responsiveness t

Interventions

  • DRUG Triamcinolone Acetonide

Trial Details

FieldValue
Enrollment Target 68 participants
Start Date 2019-11-13
Est. Completion 2025-12-24
Phase Phase 2
Emory University

1,208 total trials

What the finished NCT04002362 record still lists

NCT04002362 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 68 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (49% lower).

The record links to 0 conditions, and to 1 intervention - of which Triamcinolone Acetonide is the first listed.

NCT04002362 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04002362 about?

NCT04002362 is a clinical study titled "Symptom Clusters in Children With Exacerbation-prone Asthma". Pediatric participants with exacerbation-prone asthma will receive an intramuscular injection of triamcinolone acetonide and will be followed for 48 weeks. The study visit 2 weeks after the injection will assess the response to the study medication, while the remaining study visits will examine the ...

What is the current status of trial NCT04002362?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 68 participants. The study started on 2019-11-13. Estimated completion is 2025-12-24.

What interventions are being tested in trial NCT04002362?

The interventions under investigation include: Triamcinolone Acetonide (DRUG).

Who is sponsoring clinical trial NCT04002362?

This trial is sponsored by Emory University, which has 1,208 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04002362's enrollment target sits among peer trials

68 967th of 2000 higher than 1,027 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

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Source: ClinicalTrials.gov NCT04002362, the US trial registry maintained by the National Library of Medicine. NCT04002362 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.