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NCT04266535 Clinical Trial

TCI vs Manually Controlled Infusion of Propofol

Laparotomy Clinical Trial

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04266535
Other study ID # TCI/RHWJ
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 1, 2020
Est. completion date October 1, 2020

Study information
Verified date February 2020
Source Regional Hospital West Jutland
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial 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

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 40
Est. completion date October 1, 2020
Est. primary completion date October 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Patients to laparoscopic surgery

Exclusion Criteria:

-

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Target controlled infusion
Target controlled infusion vs manually controlled infusion

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Regional Hospital West Jutland

Outcome
Type Measure Description Time frame Safety issue
Primary Post procedural awakening Time from the surgical procedure has ended until arrival at the post anesthesia unit (PACU) 10 minutes
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