Skip to main content
OpenTrials
Completed

NCT Number: NCT03603873

Preoperative Anxiety Level, Premedications and General Anaesthetic Proceedings

Although it seems obvious that the high level of preoperative anxiety may affect intraoperative anaesthetic requirements and recovery adversely, there are several contradictory studies about this subject. Furthermore, the effects of anxiolytic premedication are actually disputed: sedative premedication is widely administered but little clinical evidence supports its use.

We want to evaluate the effects of pre-procedure anxiety for propofol needs in patients receiving general anaesthetic procedure. We also want to know if premedication is useful according to the preoperative anxiety level, in order to determine if a sub-group of patients benefit from it.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Damien JOLLY

Reims, France

About this study

This study will be carried out in solely at the institute of CHU de Reims, France (Reims Teaching Hospital) from March 2017 to May 2017. Selected patients will be over the age of 18, among those receiving general anaesthesia for surgery. Demographic data and medical history will be collected after written consent. Before the anaesthetic procedure, an APAIS questionnaire (Anxiety evaluation form) will be filled out by each patient.

The medical, anaesthetic and surgical care will not be changed. In the operating room, we will proceed with anaesthetic induction following a medical protocol according to the practice of our hospital (TCI Target Controlled Infusion or manual induction): the propofol infusion or injection is started with an initial effect-site concentration or dose and increased step by step until patients present the clinical en points defined as LOC (loss of consciousness, i.e. no response to a verbal command).

The effect-site concentration of propofol, induction time required for a loss of consciousness (LOC), and preoperative incidents will be recorded by an anaesthetist student nurse and will be recorded in a data book.

After surgery, we will record any secondary effect attributable to premedication.

The day after surgery, patients will be assessed with the EVAN-G questionnaire. Statistical analysis will be done in sub-groups with variance analysis. We will also do multivariate regression analysis according to the type of premedication, demographic data, preoperative variable and preoperative anxiety level. If the number of included patients allows it, we will do propensity score matching for premedication.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • age > 18 years old
  • surgery with general anaesthetic, programmed, in emergency or ambulatory
  • Cognitive level adequate to submit APAIS - EVANG form
  • General anaesthetic induction procedure using propofol

Exclusion criteria

  • ASA 4 level
  • Patient refusal
  • pregnancy
  • Rapid Sequence Induction (ISR)
  • General Anaesthetic induction procedure using another drug than propofol (thiopental - etomidate)

Treatment and study plan

Primary outcomes

  1. Preoperative anxiety level

    Time frame: Day 0

    this outcome will be interpreted according to the preoperative anxiety level (APAIS score)

  2. Premeds

    Time frame: Day 0

    this outcome will be interpreted according to the use or not of premeds

Sponsors and collaborators

Lead sponsor

CHU de Reims

Other

Registry information

Official study title

Preoperative Anxiety Level, Premeds and General Anaesthetic Proceedings

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Jul 27, 2018
Registry last updated
Jul 27, 2018

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.

Published trials that share one or more normalized conditions with this study.