- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04675203
Molecular Mechanisms of Tooth Eruption
March 29, 2021 updated by: University Hospital, Strasbourg, France
The main objective is to study the expression of molecules involved in tooth morphogenesis and eruption in healthy patients, and then to compare them with the results in patients with abnormalities of eruption (results obtained via a collection of biological samples of rare diseases already authorized).
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Marion STRUB
- Phone Number: +33 3 88 69 56
- Email: marion.strub@chru-strasbourg.fr
Study Locations
-
-
-
Strasbourg, France, 67091
- Les Hôpitaux Universitaires de Strasbourg
-
Contact:
- Marion STRUB
- Phone Number: +33 3 88 69 56
- Email: marion.strub@chru-strasbourg.fr
-
Principal Investigator:
- Marion STRUB
-
-
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
12 years and older (ADULT, OLDER_ADULT, CHILD)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Primary care clinic (Hôpitaux Universitaires de Strasbourg, France)
Description
Inclusion Criteria:
- Patient over 12 years old who has given his consent
- Patient whose legal representatives have given their consent for the use of operating waste destined for incineration
- Patient undergoing oral surgery at the University Hospitals of Strasbourg, at the origin of the production of surgical waste such as teeth and bone fragments
- Patient affiliated to a social security system
Exclusion Criteria:
- Refusal to participate
- Patient with chronic systemic pathology
- Patient under long-term drug treatment
- Patient presenting a rare pathology with oral manifestation
- Patient with a history of chemotherapy or head and neck radiotherapy
- Non-French speaking patient / inability to give informed information
- Patient under guardianship, curatorship or legal protection
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Normal tooth eruption
|
Tooth extraction
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Expression and localization of molecules involved in tooth eruption
Time Frame: During surgery
|
Tissues are collected at the time of surgery and transferred during the day to the laboratory for analysis
|
During surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (ANTICIPATED)
March 1, 2021
Primary Completion (ANTICIPATED)
March 1, 2021
Study Completion (ANTICIPATED)
January 1, 2023
Study Registration Dates
First Submitted
December 14, 2020
First Submitted That Met QC Criteria
December 14, 2020
First Posted (ACTUAL)
December 19, 2020
Study Record Updates
Last Update Posted (ACTUAL)
March 30, 2021
Last Update Submitted That Met QC Criteria
March 29, 2021
Last Verified
March 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 7946
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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