NCT04266535

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

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started May 2020

Shorter than P25 for all trials

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 10, 2020

Completed
2 days until next milestone

First Posted

Study publicly available on registry

February 12, 2020

Completed
3 months until next milestone

Study Start

First participant enrolled

May 1, 2020

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2020

Completed
Last Updated

February 17, 2020

Status Verified

February 1, 2020

Enrollment Period

5 months

First QC Date

February 10, 2020

Last Update Submit

February 12, 2020

Conditions

Anesthesia, IntravenousLaparotomyAirway Extubation

Outcome Measures

Primary Outcomes (1)

  • Post procedural awakening

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

    10 minutes

Study Arms (2)

TCI

Patients receiving Target Controlled Infusion (TCI) Anesthesia

Device: Target controlled infusion

MCI

Patients receiving Manually Controlled Infusion (MCI) Anesthesia

Device: Target controlled infusion

Interventions

Target controlled infusionDEVICE

Target controlled infusion vs manually controlled infusion

MCITCI

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Anestectic records

You may qualify if:

  • \- Patients to laparoscopic surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
OTHER
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

February 10, 2020

First Posted

February 12, 2020

Study Start

May 1, 2020

Primary Completion

October 1, 2020

Study Completion

October 1, 2020

Last Updated

February 17, 2020

Record last verified: 2020-02

Data Sharing

IPD Sharing
Will share
Shared Documents
STUDY PROTOCOL, CSR