Sepsis, Severe Sepsis and Septic Shock Detection by Breath Analysis

NCT03497182 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2019-05-07

No results posted yet for this study

Summary

Breath samples will be collected from patients suspected of sepsis/severe sepsis or septic shock according to hospital sepsis screening criteria in the Emergency Department.

Conditions

Interventions

DEVICE

Breath sample collection

Subject exhales into breath collection container.

Sponsors & Collaborators

  • Landon Pediatric Foundation

    lead OTHER

Principal Investigators

  • Chris Landon · Director Pediatrics

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-05-02
Primary Completion
2018-10-06
Completion
2018-10-31
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03497182 on ClinicalTrials.gov