Bone Resorption, Soft Tissue Bleeding
Conditions
Keywords
dental implants, implant neck design, immediate implants, immediate provisionalization, buccal bone thickness
Brief summary
The goal of this clinical trial is to test two different implant neck designs in 36 patients. The main question\[s\] it aims to answer are: * do triangular neck designed implants placed immediately after dental extraction have the same influence on peri-implant hard and soft tissues than regular neck designed implants at one year? * do triangular neck designed implants placed immediately after dental extraction have the same influence on peri-implant hard and soft tissues than regular neck designed implants at three years? Participants that present an unrepairable tooth on the anterior upper maxilla will be asked to take a CBCT scan in order to verify the presence of the buccal bone. Once this is verified the patients will enter in the study and the day of the surgery they will be assigned to either control or test group. * Control group: C1 round-neck implant * Test groups: V3 triangular-implant neck Researchers will compare test and control groups to see if they have the same effects on hard and soft tissues at 4 months, 1 year and 3 years.
Detailed description
Immediate implant placement is considered to be a technique-sensitive protocol with a variety of potential risks. The interface area between the neck of the implant and the abutment is critical; it can affect the treatment outcome, particularly mar-ginal bone loss (MBL) and soft tissue behavior. Traditionally, the implant neck is circu-lar in shape; however, a new triangular neck design has recently been introduced on the market, though advanced indications of this innovative design are still lacking. The objective of this randomized clinical trial was to compare the clinical and radiographic outcomes obtained after immediate placement of implants and temporization of two different neck geometries: a traditional round neck (RN) and an innovative neck with a triangular shape (TN).
Interventions
Placement of immediate implant and immediate provisionalization after tooth extraction
Sponsors
Universitat Internacional de Catalunya
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Randomized Controlled Clinical Trial
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* healthy non-smokers or light smokers (\< 10 cigarettes/day) * adults (\> 18 years of age), * need for single tooth extraction of a maxillary incisor, canine or premolar * adequate oral hygiene * ability to follow instructions and attend the required appointments * presence of a length of at least 3 mm of buccal bone measuring ≥ 0.5 mm in thickness, apical to the extraction socket * stable and intact socket walls
Exclusion criteria
* patients with acute infections in the area of interest * individuals with large occlusal discrepancies and/or occlusal overload para-functions * smokers of more than 10 cigarettes/day * patients with any medical condition or medication contraindicating dental implant treatment
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Buccal bone width (BBW) | 4 months | buccal bone width was measured by CBCT (iCAT®, Imaging Science International, LLC, Hatfield, PA, USA) at four points: at the implant neck, and at 1 mm, 2 mm and 3 mm above the implant neck. |
| Marginal bone loss (MBL) | 4 months | marginal bone loss was measured on mesial and distal aspects of the implant using intraoral standardized periapical radiographs with the parallel technique. Measurements were performed using K-Pacs Work-station (Image Information Systems, Ltd.). The distance from the implant shoulder to the first bone-implant contact was measured at the mesial and distal sites. |
| Soft tissue thickness (STT) | 4 months | the thickness of the buccal soft tissue at 3 mm and 5 mm from the gingi-val margin was measured using an endodontic file. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Bleeding on probing (BOP): | 4 months | bleeding on probing was registered at each PPD site, whether there was bleeding or not. |
| Insertion torque (IT): | day 1 | the insertion torque of the implant was measured on the day of the sur-gery with the implant motor. |
| Pink esthetic score (PES): | 4 months | this score was measured based on the Furhauser table. Maximum: 14 points / Minimum: 0 points. Higher scores mean a better outcome. |
| Crestal width (CW) | 4 months | at 3 mm and 5 mm from the gingival margin: a gauge compass was used to measure the whole width of the crestal volume, from palatal to ves-tibular wall. |
| ISQ (implant stability quotient): | day 1 | the ISQ was measured at implant placement using the Osstell device, which involves resonance frequency analysis (RFA) for measuring the fre-quency of vibration. |
| Probing pocket depth (PPD): | 4 months | probing pocket depth was measured with a Marquis Color code dental probe at 6 sites covering 360ª of the tooth: three on the buccal site and three on the palatal site of each tooth. |
Countries
Spain
Outcome results
None listed