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Clinical Trials/NL-OMON35334
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

Sponsor
Centra voor Anticonceptie, Seksualiteit en Abortus CASA

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