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OpenTrials
Active, Not Recruiting

NCT Number: NCT04984486

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

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Cabinet du Dr ALLOUCHE

Montpellier, 34000, France

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

dental implant

Device

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.

Primary outcomes

  1. the success rate of tissue integration of the implant

    Time frame: 15 years after implantation

    Integration of the implant 15 years after implantation

Secondary outcomes

  1. Change of the quality of life of patients following the recovery of a complete dentition with the OHIP- 14 score (Oral Health Impact Profile)

    Time frame: 5 years after implantation

    The quality of life of patients will be evaluate with the OHIP- 14 score (Oral Health Impact Profile) before implantation and 5 years after implantation

  2. Complication rate taking into account pain, local tenderness, infection, allergy, mobility of the implant, fracture

    Time frame: 5 years after implantation

    pain, local tenderness, infection, allergy, mobility of the implant, fracture will be collected during during the 5 years follow-up

  3. Measuring chewing function with occlusal assessment

    Time frame: 5 years after implantation

    Occlusal assessment will be performed after implantation and at 5 years follow-up

  4. Radiographic analysis of the osseointegration of the implant

    Time frame: 5 years after implantation

    A radiographic analysiswill be performed after implantation and at 5 years follow-up to evaluate the osseointegration of the implant

  5. Absence of inflammation (visual) and infection (radiographic)

    Time frame: 5 years after implantation

    Assessment of inflammation with visual examination and assessment of infection with radiographic examination 5 years after implantation

Sponsors and collaborators

Lead sponsor

Sudimplant SAS - Groupe TBR

Industry

Registry information

Important dates

Study start
2021
Primary completion
2027
Study completion
2027
First posted
Jul 30, 2021
Registry last updated
Apr 26, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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