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The Effect of Hyperoxia on Cardiac Output

M

Medical Centre Leeuwarden

Status

Completed

Conditions

Hyperoxia
Cardiac Output, Low

Study type

Observational

Funder types

Other

Identifiers

NCT03930979
nWMO270

Details and patient eligibility

About

Rational: Preoxygenation is a standard procedure before (deep) sedation in the ED. However, there is literature suggesting that too much oxygen can be harmful. One potential detrimental effect is a decrease in cardiac output due to coronary vasoconstriction. So far, it is unknown if this effect is rate dependent and if it also occurs after only a short period of hyperoxia, as patients experience during procedural sedation pre-oxygenation.

Objective: To investigate if hyperoxia has a negative effect on Cardiac index (CI) in patients undergoing procedural sedation in the ED.

Full description

Methods: In patients needing sedation for a painful condition, non-invasive measurements of CI, stroke volume and total peripheral resistance are performed using the Clearsight non-invasive cardiac output monitoring system.. Measurements will be taken at baseline, after 1,2 and 5 minutes of 15L O2/min, and then after another 2 and 5 minutes of flush rate oxygen and during the subsequent sedation.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients presenting in the ED of the Medical Center Leeuwarden (MCL) who have a painful condition for which procedural sedation is required.

Exclusion criteria

    • Cardiogenic shock (SBP<90 mmHg)
  • Procedural sedation for cardioversion
  • Pregnancy
  • General contra-indications for the procedural sedation according to local sedation protocol of the MCL.
  • Hypoxia (sat <90% or pO2 <8)) despite oxygen suppletion
  • Age < 18 years
  • Non-invasive ventilation (NIV) or intubation
  • No informed consent
  • Use of bleomycin
  • COPD GOLD III of IV
  • COPD GOLD I of II with hypercapnia (PCO2 > 6,4 kPa)
  • Patients in whom no reliable signal for Clearsight measurement can be obtained

Trial design

60 participants in 1 patient group

Clearsight measurements
Description:
All patients presenting to the ED who have a painful condition for which procedural sedation is required will undergo Clearsight measurements

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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