Telemedicine and Forensic Odontology
Sponsor
University Hospital, Montpellier (Other)
Overall Status
Recruiting
CT.gov ID
NCT05305157
Collaborator
(none)
100
1
4
24.9
Study Details
Study Description
Brief Summary
The aim of this study is to identify the expectations of experts in forensic odontology on telemedicine.
This study could improve, in multiple cases post mortem body identification.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Detailed Description
Experts in forensic odontology will have to complete a questionnaire that will reveal their expectations and knowledge on telemedicine.
Study Design
Study Type:
Observational
Anticipated Enrollment
:
100 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
National Evaluation of the Expectations of Experts in Forensic Odontology on Telemedicine
Actual Study Start Date
:
Mar 1, 2022
Anticipated Primary Completion Date
:
Jun 30, 2022
Anticipated Study Completion Date
:
Jul 1, 2022
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Experts on forensic odontology Experts on forensic odontology, members of AFIO (French Association of odontological identification) and UIO (Odontological identification Unit) |
Outcome Measures
Primary Outcome Measures
- Evaluate the knowledge [1 day]
Evaluate the knowledge expectations on telemedicine among experts on forensic odontology
- Evaluate the expectations [1 day]
Evaluate the expectations on telemedicine among experts on forensic odontology
Secondary Outcome Measures
- Highlight the key points to work in legal teleodontology [1 day]
Highlight the key points to work in legal teleodontology according to the expectations of experts
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion criteria:
- Experts in forensic odontology members of the AFIO or UIO association
Exclusion criteria:
- Dentist who not practicing forensic odontology
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Uhmontpellier | Montpellier | France | 34295 |
Sponsors and Collaborators
- University Hospital, Montpellier
Investigators
- Study Director: Camille INQUIMBERT, PhD, University Hospital, Montpellier
- Principal Investigator: Camille AMMOR, GRANDATI, resident, UH MONTPELLIER
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
University Hospital, Montpellier
ClinicalTrials.gov Identifier:
NCT05305157
Other Study ID Numbers:
- RECHMPL22_0080
First Posted:
Mar 31, 2022
Last Update Posted:
Mar 31, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Montpellier
Additional relevant MeSH terms: