TCI vs Manually Controlled Infusion of Propofol

NCT ID: NCT04266535

Last Updated: 2020-02-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-05-01

Study Completion Date

2020-10-01

Brief Summary

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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

Detailed Description

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Conditions

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Anesthesia, Intravenous Laparotomy Airway Extubation

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

OTHER

Study Groups

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TCI

Patients receiving Target Controlled Infusion (TCI) Anesthesia

Target controlled infusion

Intervention Type DEVICE

Target controlled infusion vs manually controlled infusion

MCI

Patients receiving Manually Controlled Infusion (MCI) Anesthesia

Target controlled infusion

Intervention Type DEVICE

Target controlled infusion vs manually controlled infusion

Interventions

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Target controlled infusion

Target controlled infusion vs manually controlled infusion

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

\- Patients to laparoscopic surgery

Exclusion Criteria

\-
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Regional Hospital West Jutland

OTHER

Sponsor Role lead

Responsible Party

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Niels Peter Ekeløf

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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TCI/RHWJ

Identifier Type: -

Identifier Source: org_study_id

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