Comparison and Opinion on the Safety of Teleconsultation Versus Traditional Anaesthetic Consultation in a Day Hospital

NCT ID: NCT06248060

Last Updated: 2024-04-19

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

COMPLETED

Clinical Phase

NA

Total Enrollment

300 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-02-15

Study Completion Date

2024-04-08

Brief Summary

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A pre-anaesthetic consultation is compulsory. It must be carried out at least 8 days before a scheduled medical and/or surgical operation. Its main objectives are to take the patient's history, carry out a clinical examination, select the complementary examinations that should be carried out, and inform the patient of the procedure and the type of anaesthetic proposed. In a world moving towards virtualisation, a number of medical specialities have opted for remote consultations, either by telephone or video-conferencing. Teleconsultation seems to offer greater satisfaction, not only for patients, but also for surgeons and anaesthetists. It is also associated with a reduction in the distance travelled by patients, costs and financial expenditure, with no increase in the rate of cancellation of surgery. For the first time at the Brussels University Hospital (Erasme), the anaesthesia and intensive care team will gradually introduce the system of pre-anaesthetic teleconsultation by telephone from October 2023.

The aim of our study is to evaluate the effectiveness of preanaesthetic teleconsultation at the Erasme HUB. In fact, it would be better to have results based on local expertise in order to give an answer on the effectiveness, safety and security of this innovative method, which will be officially implemented in October 2023.

Detailed Description

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Conditions

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Pre-anaesthetic Consultation

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Before - After study
Primary Study Purpose

SCREENING

Blinding Strategy

NONE

Study Groups

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Before preanaesthetic teleconsultation implementation

Group Type ACTIVE_COMPARATOR

preanaesthetic classical physical consultation

Intervention Type OTHER

Pre-anaesthetic classical consultation before teleconsultation implementation

After preanaesthetic teleconsultation implementation

Group Type EXPERIMENTAL

preanaesthetic teleconsultation

Intervention Type OTHER

Pre-anaesthetic consultation by telephone for eligible patients according to the criteria set

Interventions

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preanaesthetic classical physical consultation

Pre-anaesthetic classical consultation before teleconsultation implementation

Intervention Type OTHER

preanaesthetic teleconsultation

Pre-anaesthetic consultation by telephone for eligible patients according to the criteria set

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients scheduled for any surgery at one day hospital and who have signed the consent form.
* Pre-anaesthetic consultation by telephone.


* patients having undergone any surgery at one day hospital during the period between 01/01/2023 and 31/06/2023.
* Pre-anaesthetic consultation carried out face-to-face.
* Patients eligible for teleconsultation

Exclusion Criteria

* Participation in another clinical study within the previous month.
* Patient unable to complete the questionnaire.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Erasme University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Céline Boudart

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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boudart céline

Role: PRINCIPAL_INVESTIGATOR

HUB

Locations

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Boudart Céline

Brussels, , Belgium

Site Status

Countries

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Belgium

Other Identifiers

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SRB2023303

Identifier Type: -

Identifier Source: org_study_id

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