Telemedicine and Forensic Odontology
National Evaluation of the Expectations of Experts in Forensic Odontology on Telemedicine
1 other identifier
observational
100
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Mar 2022
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2022
CompletedFirst Submitted
Initial submission to the registry
March 22, 2022
CompletedFirst Posted
Study publicly available on registry
March 31, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2022
CompletedMarch 31, 2022
March 1, 2022
4 months
March 22, 2022
March 22, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Evaluate the knowledge
Evaluate the knowledge expectations on telemedicine among experts on forensic odontology
1 day
Evaluate the expectations
Evaluate the expectations on telemedicine among experts on forensic odontology
1 day
Secondary Outcomes (1)
Highlight the key points to work in legal teleodontology
1 day
Study Arms (1)
Experts on forensic odontology
Experts on forensic odontology, members of AFIO (French Association of odontological identification) and UIO (Odontological identification Unit)
Eligibility Criteria
Experts in forensic odontology members of the AFIO or UIO association
You may qualify if:
- \- Experts in forensic odontology members of the AFIO or UIO association
You may not qualify if:
- \- Dentist who not practicing forensic odontology
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Uhmontpellier
Montpellier, 34295, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Camille INQUIMBERT, PhD
University Hospital, Montpellier
- PRINCIPAL INVESTIGATOR
Camille AMMOR, GRANDATI, resident
UH MONTPELLIER
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 22, 2022
First Posted
March 31, 2022
Study Start
March 1, 2022
Primary Completion
June 30, 2022
Study Completion
July 1, 2022
Last Updated
March 31, 2022
Record last verified: 2022-03