Dental CariesNCT05305157
Telemedicine and Forensic Odontology
An observational study of Dental Caries, run by University Hospital, Montpellier at 1 site in France.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Dental Caries
- How many people
- 100 participants
- Where
- 1 siteFrance
- Study dates
- 1 Mar 2022to 1 Jul 2022
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Experts in forensic odontology members of the AFIO or UIO association
Who may be able to join
- Experts in forensic odontology members of the AFIO or UIO association
Who cannot join
- Dentist who not practicing forensic odontology
Trial locations and contacts
1 site in 1 country.
Nicolas GIRAUDEAU, PhD contact
France1 site, 1 recruiting
- Recruiting
Uhmontpellier
Montpellier, 34295
Camille INQUIMBERT, Phd, 666957674 ext. 33, camille.inquimbert@gmail.com
Nicolas GIRAUDEAU, PhD
About this study
Official title: National Evaluation of the Expectations of Experts in Forensic Odontology on Telemedicine
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.
Read the detailed description
Experts in forensic odontology will have to complete a questionnaire that will reveal their expectations and knowledge on telemedicine.
- Conditions
- Dental Caries
- Keywords
- Public Health, Forensic odontology, Telemedicine, Identification post mortem, dentist who is an forensic odontology expert, member of the AFIO or UIO
- Medical subject headings
- Dental Caries
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Experts on forensic odontology | Experts on forensic odontology, members of AFIO (French Association of odontological identification) and UIO (Odontological identification Unit) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Evaluate the knowledge
Evaluate the knowledge expectations on telemedicine among experts on forensic odontology
Measured: 1 day
Evaluate the expectations
Evaluate the expectations on telemedicine among experts on forensic odontology
Measured: 1 day
Secondary outcomes (1)
Highlight the key points to work in legal teleodontology
Highlight the key points to work in legal teleodontology according to the expectations of experts
Measured: 1 day
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted31 Mar 2022
- Study start1 Mar 2022
- Primary completion30 Jun 2022 (estimated)
- Study completion1 Jul 2022 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Dental CariesStudies of the same condition, open and under way.
- More trials run by University Hospital, MontpellierThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Prospective
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University Hospital, Montpellier
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Camille INQUIMBERT, PhD, Study director, University Hospital, MontpellierCamille AMMOR, GRANDATI, resident, Principal investigator, UH MONTPELLIER
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05305157
- Sponsor's protocol ID
- RECHMPL22_0080
- Status last verified
- Mar 2022
- First submitted
- 22 Mar 2022
- Last updated
- 31 Mar 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: NC
Study at a glance
From the registry record, last updated by the sponsor on 31 Mar 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- National Evaluation of the Expectations of Experts in Forensic Odontology on Telemedicine
- ClinicalTrials.gov ID
- NCT05305157
- Acronym / sponsor ID
- RECHMPL22_0080
- Conditions
- Dental Caries
- Keywords
- Public Health, Forensic odontology, Telemedicine, Identification post mortem, dentist who is an forensic odontology expert, member of the AFIO or UIO
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- University Hospital, MontpellierUniversity, hospital or other
- Study start
- 1 Mar 2022 (actual)
- Primary completion
- 30 Jun 2022 (estimated)
- Study completion
- 1 Jul 2022 (estimated)
- First posted
- 31 Mar 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
Experts in forensic odontology will have to complete a questionnaire that will reveal their expectations and knowledge on telemedicine.
Study design
- Observational model
- Case only
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Experts on forensic odontology | – | –Experts on forensic odontology, members of AFIO (French Association of odontological identification) and UIO (Odontological identification Unit) |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Experts in forensic odontology members of the AFIO or UIO association
Key inclusion criteria (1 listed)
- Experts in forensic odontology members of the AFIO or UIO association
Key exclusion criteria (1 listed)
- Dentist who not practicing forensic odontology
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Evaluate the knowledge
Time frame: 1 day
Evaluate the knowledge expectations on telemedicine among experts on forensic odontology
Evaluate the expectations
Time frame: 1 day
Evaluate the expectations on telemedicine among experts on forensic odontology
1 secondary outcome
Highlight the key points to work in legal teleodontology
Time frame: 1 day
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Mar 2022.
- Individual participant dataSharing planned: Undecided. NC
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Nicolas GIRAUDEAU, PhD contact
Camille INQUIMBERT, PhD study director
University Hospital, Montpellier
Camille AMMOR, GRANDATI, resident principal investigator
UH MONTPELLIER
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Dental Caries, run by University Hospital, Montpellier at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 31 Mar 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Camille INQUIMBERT, PhD (666957674 ext. 33, camille.inquimbert@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Evaluate the knowledge (time frame: 1 day). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Mar 2022.