Is Pre-anaesthetic Teleconsultation a Safe Alternative to Traditional Pre-anaesthetic Consultation?
1 other identifier
interventional
200
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 9, 2024
CompletedStudy Start
First participant enrolled
January 18, 2024
CompletedFirst Posted
Study publicly available on registry
January 29, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
March 30, 2024
CompletedApril 19, 2024
April 1, 2024
2 months
January 9, 2024
April 18, 2024
Conditions
Outcome Measures
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.
at the end of the procedure
Secondary Outcomes (2)
Satisfaction scores reported on LIKERT scale (1-5)
before the procedure
Pre-operative anxiety scorereported on LIKERT scale (1-5)
before the procedure
Study Arms (2)
Before preanaesthetic teleconsultation implementation
ACTIVE COMPARATORAfter preanaesthetic teleconsultation implementation
EXPERIMENTALInterventions
Pre-anaesthetic consultation by telephone for eligible patients according to the criteria set
Pre-anaesthetic classical consultation before teleconsultation implementation
Eligibility Criteria
You may qualify if:
- Patients scheduled for gastroscopy and/or colonoscopy and who have signed the consent form.
- Pre-anaesthetic consultation by telephone.
- Procedure scheduled in day hospital.
- patients having undergone gastroscopy and/or colonoscopy during the period between 01/01/2023 and 31/06/2023.
- Pre-anaesthetic consultation carried out face-to-face.
- Day hospital procedure.
- Patients eligible for teleconsultation
You may not qualify if:
- Participation in another clinical study within the previous month.
- Patient unable to complete the questionnaire.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Boudart Céline
Brussels, 1070, Belgium
Study Officials
- PRINCIPAL INVESTIGATOR
boudart céline
HUB
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- SCREENING
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 9, 2024
First Posted
January 29, 2024
Study Start
January 18, 2024
Primary Completion
March 30, 2024
Study Completion
March 30, 2024
Last Updated
April 19, 2024
Record last verified: 2024-04
Data Sharing
- IPD Sharing
- Will not share