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N/A Completed N=43 Randomized Double-blind Treatment

HFCWO in Hospitalized Asthmatic Children

Asthma · Status Asthmaticus
Source: ClinicalTrials.gov NCT00722020 ↗
Enrolled (actual)
43
Serious AEs
0.0%
Results posted
Nov 2015
Primary outcomePrimary: The Primary Endpoint Will be Time to Readiness for Discharge. — 1.74; 1.75 days

Summary

To determine whether or not high frequency chest wall oscillation (in the form of the VestTM) is superior to regular asthma therapy in the management of children hospitalized with moderate to severe asthma.

Outcome Measures

OutcomeResultp-value
PRIMARY
The Primary Endpoint Will be Time to Readiness for Discharge.
1.74; 1.75
SECONDARY
Secondary Endpoint Total Hospital Length of Stay
2.5; 2.5

Eligibility Criteria

Inclusion Criteria

  • Any pediatric patient between the ages of 18 months and 18 years admitted to Winthrop University Hospital's pediatric floor or intensive care unit with a diagnosis of asthma or reactive airway disease

Exclusion Criteria

  • Patients with chronic, comorbid respiratory conditions (e.g., cerebral palsy, cystic fibrosis)
  • Those who regularly use HFCWO
  • Any patient exhibiting an absolute contraindication to HFCWO therapy
  • Absolute contraindications to using HFCWO include head and neck injury prior to stabilization, and active hemorrhage with hemodynamic instability
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00722020). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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