NL-OMON35334CompletedNot Applicable
Assessment of Capnography in Monitoring Patients during Deep Sedation with Propofol - Capnography during deep sedation
Centra voor Anticonceptie, Seksualiteit en Abortus CASA0 sites440 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 440
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18 to 99 (—)
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
- •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
Investigators
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