Assessment of Capnography in Monitoring Patients during Deep Sedation with Propofol

Assessment of Capnography in Monitoring Patients during Deep Sedation with Propofol - Capnography during deep sedation

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON35334

Enrollment

440

Registered

2010-03-25

Start date

2010-04-21

Completion date

Unknown

Last updated

2024-08-12

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

Conditions

iatrogeen veroorzaakte hypoventilatie door sedatie alveolar hypoventilation oxygen debt

Interventions

The intervention comprises application of capnography during deep sedation with propofol. In the intervention arm, patients* breathing is additionally monitored with capnography. If alveolar hypoven

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Age 18 years or older Abortion procedures performed until 22 weeks of gestational age American Society of Anaesthesiologists (ASA) classes I to II (normal healthy patients or patients with a mild systemic disease) Ability to give written informed consent.

Exclusion criteria

Exclusion criteria: Inability to provide written informed consent History of allergic reactions to propofol, soybeans or egg proteins American Society of Anaesthesiologists (ASA) classes III to V (patients with a severe systemic disease, with or without constant threat to life, or moribund patients) Sleep apnea syndrome Patients with known seizure disorders

Design outcomes

Primary

Measure	Time frame
The primary outcome for both groups is the number of patients with oxygen saturations to	—

Secondary

Measure	Time frame
Secondary study outcomes are the number of patients with saturations to	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)