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CompletedNCT06248060Updated Apr 19, 2024

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

An interventional study of preanaesthetic classical physical consultation and preanaesthetic teleconsultation in Pre-anaesthetic Consultation, sponsored by Erasme University Hospital. Completed at 1 site in Belgium. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2024-04-19.

Sponsored by Erasme University Hospital · Not applicable, Interventional, and Screening

Phase
Not applicable
Study type
Interventional
Enrollment
300
Allocation
Non-randomized
Ages
18 Years to 65 Years
Sex
All
01

Study 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.

02

Conditions studied

  • Pre-anaesthetic Consultation
03

In context

Lead sponsor

Erasme University Hospital is the lead sponsor of 178 studies on the registry; 34 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 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 31/06/2023.
  • Pre-anaesthetic consultation carried out face-to-face.
  • Patients eligible for teleconsultation

Exclusion criteria

Exclusion Criteria:

  • Participation in another clinical study within the previous month.
  • Patient unable to complete the questionnaire.
05

Study design

Phase
Not applicable
Primary purpose
Screening
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
300 participants (actual)

Study arms

  • Active comparator
    Before preanaesthetic teleconsultation implementation

    Other: preanaesthetic classical physical consultation

  • Experimental
    After preanaesthetic teleconsultation implementation

    Other: preanaesthetic teleconsultation

Interventions

  • Otherpreanaesthetic classical physical consultation

    Pre-anaesthetic classical consultation before teleconsultation implementation

  • Otherpreanaesthetic teleconsultation

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

06

What researchers measure

Primary outcomes

  1. Score of Patient endangerment (0-4)

    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.

    Time frame: at the 1 day of surgery

Secondary outcomes

  1. Satisfaction scores reported on LIKERT scale (1-5)

    How do you feel about the anaesthetic teleconsultation? 1 = Very satisfied; 2 = Satisfied; 3 = Neither satisfied nor dissatisfied; 4 = Not very satisfied; 5 = Not at all satisfied.

    Time frame: Baseline (before the procedure)

  2. Pre-operative anxiety scorereported on LIKERT scale (1-5)

    How would you rate your level of anxiety? 1 = Not at all anxious; 2 = Slightly anxious; 3 = Moderately anxious; 4 = Somewhat anxious; 5 = Very anxious

    Time frame: Baseline (before the procedure)

07

Study locations

1 site
  • Boudart Céline
    Bruxelles, 1070, Belgium
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 19, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06248060
Lead sponsor
Erasme University Hospital
Responsible party
Céline Boudart (Principal Investigator, Erasme University Hospital) — Principal investigator
First posted
Feb 8, 2024
Start date
Feb 15, 2024
Primary completion
Apr 8, 2024
Completion
Apr 8, 2024
Last update
Apr 19, 2024

Study contacts

boudart céline
principal investigator · HUB

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Apr 2024. You cannot join it, but the record below documents what was studied.

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