A Randomized Clinical Trial of the Effectiveness of Ventilation by Oxylator EMX versus Bag-Valve Device in pre-hospital emergency patients.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON23375

Enrollment

200

Registered

2005-09-08

Start date

2005-05-02

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

All emergency conditions that require mask ventilation.

Interventions

1. Mask ventilation with Oxylator EMX or Bag-valve device

2. Measuring periferal saturation and end-tidal CO2 with device.

Eligibility

Inclusion criteria

Inclusion criteria: EMS patients age > 18y requiring mask ventilation.

Exclusion criteria

Exclusion criteria: 1. Cardiac arrest; 2. Pregnancy.

Design outcomes

Primary

Measure	Time frame
1. Periferal oxygen saturation; 2. End tidal carbon dioxide (CO2).	—

Secondary

Measure	Time frame
1. Survival to hospital; 2. Hospital O2 saturation & ETCO2; 3. Hospital Bloodgas.	—

Contacts

Public ContactB. Drinkwaard

St. Elisabeth Hospital, P.O. Box 90151

+31 (0)13 5391313

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)