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Clinical Trials/NCT04266535
NCT04266535
Unknown
Not Applicable

TCI vs Manually Controlled Infusion of Propofol in Patients Sceduled for Laparoscopic Surgery; a Case-control Study

Regional Hospital West Jutland0 sites40 target enrollmentMay 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anesthesia, Intravenous
Sponsor
Regional Hospital West Jutland
Enrollment
40
Primary Endpoint
Post procedural awakening
Last Updated
6 years ago

Overview

Brief Summary

Anesthesia records for patients anesthetized with target controlled infusion of propofol and remifentanil will be matched with patients anesthezied with manyally controlled infusion.

The aim of the study is to verify differences in time to extubation and amount of drugs used.

anesthetize

Registry
clinicaltrials.gov
Start Date
May 1, 2020
End Date
October 1, 2020
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Regional Hospital West Jutland
Responsible Party
Principal Investigator
Principal Investigator

Niels Peter Ekeløf

Principal Investigator

Regional Hospital West Jutland

Eligibility Criteria

Inclusion Criteria

  • Patients to laparoscopic surgery

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Post procedural awakening

Time Frame: 10 minutes

Time from the surgical procedure has ended until arrival at the post anesthesia unit (PACU)

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