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OpenTrials
Completed

NCT Number: NCT02077478

Total Intravenous Anesthesia: TCI Versus MCI

test the following differences between Schinder's Target Controlled Infusion (TCI ) model and manually controlled infusion (MCI) :

* remifentanil and propofol total dose given * incidence of awareness or inadequate anesthesia * number of rescue dose given

Completed

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

0532206570

Ferrara, 44121, Italy

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients undergoing breast or thyroid surgery

Exclusion criteria

  • BMI > 35
  • Surgery shorter than 30 minutes
  • Patients with history of: alcol or drug abuse, kidney or liver failure, cardiovascular disease

Treatment and study plan

Remifentanil and propofol administration using TCI

Device

Remifentanil and propofol administration using MCI

Device

Primary outcomes

  1. incidence of awareness or inadequate anesthesia

    Time frame: every 3 minutes till the end of surgery

Secondary outcomes

  1. remifentanil and propofol total dose given

    Time frame: every 30 minutes till the end of surgery

Sponsors and collaborators

Lead sponsor

Università degli Studi di Ferrara

Other

Registry information

Official study title

Total Intravenous Anesthesia: TCI Versus MCI, Unresolved Question

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
Mar 4, 2014
Registry last updated
Sep 5, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.