CompletedN/AOther
Ketofol Versus Propofol for Sedation in Cholangiopancreatography for ASA III and ASA IV Patients.
Sponsored by Centro Hospitalar Universitário Lisboa Norte
NCT ID
NCT05473949
Target Enrollment
102 participants
Start Date
2016-10-01
Est. Completion
2017-03-31
About This Study
This study is a double blind randomized controlled trial. The investigators randomized ASA III and IV patients who underwent cholangiopancreatography. The investigators gave Propofol or Ketofol and compared the outcomes. The primary outcome was security (respiratory depression / hypoventilation).
Conditions Studied
Interventions
- •Profofol for Sedation in Cholangiopancreatography for ASA III and ASA IV Patients
- •Ketofol for Sedation in Cholangiopancreatography for ASA III and ASA IV Patients
Eligibility
Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria: * 18 years old * ASA III and IV * Submitted to retrograde cholangiopancreatography Exclusion Criteria: * Patient refuse * ASA I, II and V * Ketamine contraindications * Allergies to Propofol, Ketamine, dexamethasone, paracetamol, metamizole, ondanseteon or other. * General anesthesia necessary I * Incapacitaty to sign or absence of patient legal representation.