In Vivo Clinical Investigation of the Safety and Performance of Dental Implants TBR® Bone Level
1 other identifier
observational
138
1 country
1
Brief Summary
Partial or total edentulousness has a significant impact on quality of life both functionally and aesthetically. TBR® Bone Level Implants allow the patient to prevent bone resorption and maintain facial tissue and musculature support. At the functional level, the patient who benefits from implant treatment regains normal masticatory function with all the benefits on the quality of life that this can bring him. Due to the osseointegration of the implant and the biocompatibility of the materials used, the implant treatment remains effective in the long term and makes it possible to maintain the aesthetics of the smile.
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 Sep 2021
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 21, 2021
CompletedFirst Posted
Study publicly available on registry
July 30, 2021
CompletedStudy Start
First participant enrolled
September 27, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 1, 2027
April 26, 2024
April 1, 2024
5.8 years
July 21, 2021
April 25, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
the success rate of tissue integration of the implant
Integration of the implant 15 years after implantation
15 years after implantation
Secondary Outcomes (5)
Change of the quality of life of patients following the recovery of a complete dentition with the OHIP- 14 score (Oral Health Impact Profile)
5 years after implantation
Complication rate taking into account pain, local tenderness, infection, allergy, mobility of the implant, fracture
5 years after implantation
Measuring chewing function with occlusal assessment
5 years after implantation
Radiographic analysis of the osseointegration of the implant
5 years after implantation
Absence of inflammation (visual) and infection (radiographic)
5 years after implantation
Interventions
The procedure used to accomplish its intended use is as follows : * The recipient implant site is prepared using a drilling sequence, then the implant is placed at the crestal level * After a period of osseointegration of the implant, a transgingival healing screw is placed to allow the healing of soft tissues. After this healing phase, the final prosthesis will be loaded on the implant.
Eligibility Criteria
Patient partially or totally toothless
You may qualify if:
- Patient 18 years of age or older
- Patient who has completed bone growth
- Patient informed and willing to participate in the study
- Partially or totally toothless patient who will be implanted with the TBR® Bone Level implant(s) for the prospective cohort
- Patient implanted with the TBR® Bone Level implant(s) before June 2011 for the retrospective cohort
You may not qualify if:
- Pregnant or lactating women
- Patient with bone disease of the head and neck region
- Patient refusing to participate in the study
- Patient with at least one contraindication to implantation
- Patient on osteoporosis treatment with Biphosphonates or Denosumab.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cabinet du Dr ALLOUCHE
Montpellier, 34000, France
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Laurent ALLOUCHE, Dr
Cabinet Dentaire du Dr Laurent ALLOUCHE
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 21, 2021
First Posted
July 30, 2021
Study Start
September 27, 2021
Primary Completion (Estimated)
July 1, 2027
Study Completion (Estimated)
July 1, 2027
Last Updated
April 26, 2024
Record last verified: 2024-04
Data Sharing
- IPD Sharing
- Will not share