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Clinical Trials/NCT06248060
NCT06248060CompletedNot Applicable

Comparison and Opinion on the Safety of Teleconsultation

Erasme University Hospital2 sites in 1 country300 target enrollmentStarted: February 15, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
300
Locations
2
Primary Endpoint
Score of Patient endangerment (0-4)

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Screening
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • for prospective group (AFTER):
  • Patients scheduled for any surgery at one day hospital and who have signed the consent form.
  • Pre-anaesthetic consultation by telephone.
  • Inclusion Criteria for retrospective group (BEFORE):
  • patients having undergone any surgery at one day hospital during the period between 01/01/2023 and 31/06/
  • 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.

Outcomes

Primary Outcomes

Score of Patient endangerment (0-4)

Time Frame: at the 1 day of surgery

Patient endangerment : 0 = Nothing to report; 1 = Lack of information but no danger to the patient; 2 =Lack of information and reduced safety but intervention maintained; 3 = Too great a risk to the patient.

Secondary Outcomes

  • Pre-operative anxiety scorereported on LIKERT scale (1-5)(Baseline (before the procedure))
  • Satisfaction scores reported on LIKERT scale (1-5)(Baseline (before the procedure))

Investigators

Sponsor
Erasme University Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Céline Boudart

Principal Investigator

Erasme University Hospital

Study Sites (2)

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