Evaluation of the Satisfaction of Patients Coming "on Foot" in the Operating Room — Bloc3D  

Surgery Clinical Trial

Official title: Evaluation of the Satisfaction of Patients Coming "on Foot" in the Operating Room (Standing, Dignified, Relaxed)

Status Completed

Clinical Trial Summary

Ambulatory surgery is currently experiencing unprecedented growth and is becoming the standard of care compared to traditional hospitalization. Without mentioning the obvious financial gains, the benefits of ambulatory care essentially lie in optimised perioperative comfort. This comfort is due to a limited period of stay (< 12 hours) and to the proactive action of the care providers.

In this context, the optimization of the whole patient's journey during the perioperative period has been reviewed and adapted to personalized management within healthcare facilities. For more than a year now, multimodal approaches such as early rehabilitation have been undertaken, including

• morning admission with an innovative principle of "3D" patient (standing, dignified, relaxed)

• no premedication, wearing glasses and wigs,

• Drinking on the morning of the intervention (2H before admission),

• Walking to the block on foot (or in a wheelchair), return adapted to the wheelchair and no longer in a stretcher,

• fast resumption of feeding.

Currently, in the investigator's various institutions, several modes of transport to the operating theatres coexist. The purpose of this observational study is to evaluate this optimization of perioperative management "3D mode", in particular the mode of transport.

The main objective is to determine the level of patient satisfaction with this management using a standardized quality questionnaire: the "EVAN" questionnaire. This questionnaire contains 22 items allowing a global analysis of patient satisfaction. This questionnaire is already routinely conducted in many institutions. The EVAN questionnaire will be supplemented by questionnaires assessing the level of perioperative anxiety. They will be initiated into the anesthesia consultation, and finalized on the day of the surgery.

Clinical Trial Description

n/a

Related Conditions & MeSH terms

• Anesthesiology
• Satisfaction, Patient
• Surgery

• NCT number: NCT04453176
• Study type: Observational
• Source: Centre Hospitalier Universitaire de Nimes
• Status: Completed
• Start date: February 25, 2019
• Completion date: February 28, 2020