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N/A Completed N=191 Randomized Diagnostic

A Randomized Controlled Trial of Lung Ultrasound Compared to Chest X-ray for Diagnosing Pneumonia in the Emergency Department

Source: ClinicalTrials.gov NCT01654887 ↗
Enrolled (actual)
191
Serious AEs
0.0%
Results posted
Mar 2017
Primary outcomePrimary: Percentage of Participants For Whom CXR Was Not Needed to Diagnose Pneumonia — 38.8; 0 percentage of participants

Summary

The primary objective of this study is to determine if lung ultrasound (LUS) can replace chest x-ray (CXR) when evaluating patients with possible pneumonia. Specifically, we are looking for an overall reduction of CXR when LUS is used first. Our null hypothesis is that LUS cannot replace CXR for diagnosing pneumonia. Our alternate hypothesis is that LUS can replace CXR for diagnosing pneumonia. Our secondary objectives include: (1) a comparison of unscheduled healthcare visits after the index Emergency Department (ED) visit between those subjects who undergo CXR first and those who undergo LUS first, (2) an evaluation of the rate of antibiotic use between the two groups, (3) a comparison of the admission rates, and (4) a comparison of the length of stay in the Emergency Department between the two groups.

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants For Whom CXR Was Not Needed to Diagnose Pneumonia
38.8; 0
PRIMARY
Percentage of Participants Whose Pneumonia Was Missed by LUS or CXR
0.0; 0.0
SECONDARY
Comparison of Unscheduled Healthcare Visits
8.7; 11.4
SECONDARY
Percentage of Participants With Antibiotic Use
37.9; 27.3
SECONDARY
Percentage of Participants Who Had Hospital Admission.
19.4; 17.0
SECONDARY
Comparison of the Length of Stay in the ED
153; 180

Eligibility Criteria

Inclusion Criteria

  • All patients who present to the ED with respiratory symptoms suspicious for pneumonia
  • In whom the treating physician believes would benefit from diagnostic imaging

Exclusion Criteria

  • Patients who arrive at the ED with a previously performed CXR
  • Unstable patients with life-threatening injuries who require ongoing resuscitation
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01654887). 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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