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Clinical Trials/NL-OMON48393
NL-OMON48393
Completed
N/A

Comparison of peripheral venous and arterial blood gas in management of patients with respiratory complaints in the emergency department. - Blood Gas Comparison trial (BGC trial)

Zuyderland Medisch Centrum0 sites155 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Zuyderland Medisch Centrum
Enrollment
155
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational invasive

Investigators

Sponsor
Zuyderland Medisch Centrum

Eligibility Criteria

Inclusion Criteria

  • Patients (\* 18 years) presenting in the ED with dyspnoea, respiratory rate \>
  • 20/min or peripheral oxygen saturation \< 95%, a reliable saturation measured by
  • pulse oximetry (measured with the Philips IntelliVue MP30 patient monitor, a
  • reliable measurement is defined by pulsatile flow with a perfusion indicator
  • value above 0\.3\) and an indication, determined by the treating physician, to
  • determine the acid\-base, ventilation and oxygenation status by arterial blood

Exclusion Criteria

  • A potential subject who meets any of the following criteria will be excluded
  • from participation in this study:
  • \- Not capable to give informed consent within reasonable time after
  • stabilisation and abating of the accompanying psychological stress, and no
  • representative available to give informed consent on behalf of the patient.
  • \- Arterial blood gas results are required for other reasons than determining
  • the acid\-base, ventilation and oxygenation status, such as determining the
  • alveolar to arterial oxygen gradient (A\-a gradient).
  • \- No physician or qualified nurse available for ABG sampling.
  • \- Failed ABG or VBG sampling after two attempts.

Outcomes

Primary Outcomes

Not specified

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