In Vivo Clinical Investigation of the Safety and Performance of Dental Implants TBR® Bone Level

NCT ID: NCT04984486

Last Updated: 2024-04-26

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Total Enrollment: 138 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-09-27
• Study Completion Date: 2027-07-31

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.

Detailed Description

Many adults have one or more missing teeth. The negative consequences of partial or total edentulousness are numerous in the orofacial sphere:

• Edentulousness causes a strong aesthetic deficit due to the lack of support of facial tissues and musculature;
• Edentulousness generates a functional deficit that can have significant repercussions on the nutritional status of the affected subject;
• Edentulousness is accompanied by bone resorption of the jawbones which is inevitable in the absence of implant treatment;
• In addition, the resulting feelings of discomfort and fragility are experienced as a real psychological handicap by the patient, partially or totally edentulous, which can then have significant repercussions on his social life.

TBR® Bone Level implants are intended for placement in the maxillary or mandibular arch in partially or completely edentulous patients for prosthetic restoration in the following cases:

• Single edentulousness,
• Intercalary edentulousness,
• Terminal edentulousness,
• Total edentulousness.

The following clinical conditions must be observed before placing a dental implant:

• Sufficient quality and volume of bone support;
• Healthy oral condition;
• no contraindications for implant setting

The expected benefits of this surgery are to improve the quality of life of patients, to recover the chewing function and the aesthetics of the smile.

Conditions

Edentulous

Study Design

• Observational Model Type: OTHER
• Study Time Perspective: CROSS_SECTIONAL

Interventions

dental implant

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.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• 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

Exclusion Criteria

• 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.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sudimplant SAS - Groupe TBR

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Laurent ALLOUCHE, Dr

Role: PRINCIPAL_INVESTIGATOR

Cabinet Dentaire du Dr Laurent ALLOUCHE

Locations

Cabinet du Dr ALLOUCHE

Montpellier, , France

Countries

France

Other Identifiers

2019-A01913-54

Identifier Type: -

Identifier Source: org_study_id