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

Anesthesia

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.

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source