- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04583865
Feasibility and Quality of TeleConsultation in Pediatric Anesthesia (TéléCCCAP)
March 10, 2026 updated by: University Hospital, Toulouse
Assessment of the Feasibility and Quality of the Consultation by TeleConsultation in Pediatric Anesthesia in the Context of the Covid 19 Pandemic
Teleconsultation (TLC) being a new method of anesthesia consultation, deployed as an emergency in healthcare facilities in the Covid context, it has never been evaluated either in terms of feasibility or in terms of quality.
An initial assessment will highlight the pitfalls and difficulties encountered and suggest areas for improvement.
Study Overview
Detailed Description
The evaluation of teleconsultation in pediatric anesthesia, a new consultation method developed in the context of COVID for several weeks, appears necessary and will be a first inventory after its implementation in France.
Analysis of the data collected in this study will allow us to propose technical, medical and organizational solutions to optimize the positioning and practical use of TLC for patients and care facilities.
This assessment step seems imperative if the Covid context persists over time but could also be useful for the development of TLC outside the Covid context.
Study Type
Observational
Enrollment (Actual)
848
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Bordeaux, France
- CHU Bordeaux
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Caen, France
- CHU de Caen
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Lyon, France
- CHUde Lyon
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Montpellier, France
- CHU de Montpellier
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Nice, France
- Chu de Nice
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Paris, France
- AP-HP Robert Debré
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Paris, France
- AP-HP Necker
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Rennes, France
- CHU de Rennes
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Saint-Denis, France
- CHU de la réunion
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Tarbes, France
- CH de Tarbes
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Toulouse, France, 31000
- UHToulouse
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
3 years to 14 years (Child, Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
patients under the age of 18 requiring an anesthesia consultation for an act requiring anesthesia
Description
Inclusion Criteria:
- All patients under the age of 18 requiring an anesthesia consultation for an act requiring anesthesia
- whose deprogramming in the context of the Covid 19 pandemic would lead to a loss of opportunity for the patient,
- Or whose programming in the context of the Covid 19 pandemic is in accordance with the recommendations made in field of the Professional Practice Recommendations
- And for which the family and the anesthetist have agreed to carry out the consultation by telemedicine
Exclusion Criteria:
- Patient whose anesthesia consultation is performed face-to-face as a first-line decision
- Family refusing teleconsultation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
teleconsultation
Patient with teleconsultation of pre-anesthesia
|
In the pandemic period linked to COVID, pediatric pre-anesthesis consultations should preferably be carried out by teleconsultation.
This is to assess the effectiveness of these teleconsultation and the satisfaction of parents.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
assess the feasibility of teleconsultation (TLC) in pediatric anesthesia in France in the context of the COVID 19 pandemic.
Time Frame: 3 months
|
The feasibility of anesthesia TLC will be assessed by the failure rate of anesthesia TLC, defined by the conversion rate to degraded TLC (use of an unsecured video medium such as WhatsApp or simple audio communication without video support) or in face-to-face consultation
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: KERN Delphine, MD, University Hospital, Toulouse
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 23, 2020
Primary Completion (Actual)
September 14, 2021
Study Completion (Actual)
November 2, 2022
Study Registration Dates
First Submitted
October 7, 2020
First Submitted That Met QC Criteria
October 9, 2020
First Posted (Actual)
October 12, 2020
Study Record Updates
Last Update Posted (Actual)
March 13, 2026
Last Update Submitted That Met QC Criteria
March 10, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RC31/20/0220
- 2020-A02275-34 (Registry Identifier: French ANSM register)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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