Phase
Condition
Lung Injury
Depression
Respiratory Failure
Treatment
Sedation using only Propofol.
Sedation using combination of Propofol and Fentanyl.
Clinical Study ID
Ages 18-65 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Scheduled therapeutic or diagnostic colonoscopy with sedation
Supine or lateral decubitus position
Age 18-65
American Society of Anesthesiologists (ASA) physical status classification system 1-2
Informed consent signed
Exclusion
Exclusion Criteria:
Planned frequent use of electrocoagulation
Contact allergy for adhesive pads, excessive thoracic hair or other problem withpads
contraindication of using Propofol or Fentanyl
Incapability to understand the informed consent
Study Design
Study Description
Connect with a study center
Military University Hospital Prague
Praha, 16209
CzechiaSite Not Available


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