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NCT02781363 Clinical Trial

Can the Thoracic Replace the Conventional Radiography for the Diagnosis of Acute Pneumonia in Children?

Pneumonia Clinical Trial

Official title:
Can the Thoracic Replace the Conventional Radiography for the Diagnosis of Acute Pneumonia in Children?

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT02781363
Other study ID # 2015/51-PED-HGC
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date January 1, 2016
Est. completion date June 1, 2016

Study information
Verified date August 2022
Source Hospital Universitari General de Catalunya
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The Thoracic ultrasound is a safer and sensitive technique than conventional radiography because it detects less than 1 cm pneumonic consolidations and minimal pleural effusions. The main objective is to evaluate the efficacy of thoracic ultrasound performed by unskilled personnel in the emergency service prdiatricas to diagnose pneumonia in children.

Description:

Diagnostic test evaluation.The sample collected sequentially until an exact size . Given the safety of the technique, which involves no risk to patient management and the possibility of generating a type II error by premature study discontinuation , we have no plans to make any interim analyzes .

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date June 1, 2016
Est. primary completion date April 30, 2016
Accepts healthy volunteers No
Gender All
Age group 3 Months to 14 Years
Eligibility Inclusion Criteria: - fever above 38 degrees - tachypnea - Difficulty breathing - Side tip pain - pathological auscultation Exclusion Criteria: - < 3 months> 14 years - Background of Prematurity - Rewalizados imaging studies in the last 7 days - Any chronic respiratory process - congenital heart diseases - hemodynamic instability - Diagnosis of pneumonia in the last 3 months - Refusal of relatives to participate in the study

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Thoracic ultrasound

• CXR

Locations
Country Name City State
Spain Hospital UNiversitari General de Catalunya Sant Cugat del Vallès Catalonia

Sponsors (1)
Lead Sponsor Collaborator
Hospital Universitari General de Catalunya

Country where clinical trial is conducted

Spain, 

Outcome
Type Measure Description Time frame Safety issue
Primary coincidence between the ultrasound image and conventional radiography images compatible with pneumonic consolidations in sonography and radiography . Coincidence between evaluators 1 day
Secondary additional workload Time (minutes) between the test requested and the results are obtained for both diagnostic tests 1 day
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