Clinical Trials Logo

Clinical Trial Summary

40 consecutive adult patients, requiring the insertion of dental implants in the aesthetic area (from second premolar to second premolar) will be enrolled in the study. At the time of surgery, a full thickness flap will be elevated, the implant bed will be prepared according to the manufacturer's instruction and the implants will be then seated into the bone. T0 corresponds to the time of implant insertion, T1 to the time of healing abutment's connection (T0=T1 for single stage implants), and T2 corresponds to 1-year follow-up from healing abutment's connection.

Cone Beam Computed Tomography (CBCT) scans will be taken immediately after abutment connection (T1) and 1-year after (T2). The midsagittal cut of each implant will be identified, and measurements will be made at predetermined levels. Horizontal facial bone thickness (HFBT) and Vertical facial bone level (VFBL) will be measured. HFBT will be measured at 0, 3, 6 and 9 mm apical to the implant platform. VFBL wil be the perpendicular distance from the implant platform to the most coronal point of the facial bone. Changes between T1 and T2 will be calculated.


Clinical Trial Description

The long term results and benefit of implant insertion in the aesthetic area have been well documented.

In the past few years, facial dimensional changes to the alveolar process following implant placement are object os study for both humans and animals investigations Recent studies suggest that platform switching decreases bone loss by 30% to 50%. It seems that the creation of a biologic width affects peri-implant bone loss to a significant extent and that platform switching is effective when the mucosal thickness allows the establishment of an horizontal biologic width.

A new implant with an hybrid surface (T3) has been recently launched by Biomet 3i.Aim of the present study will be to evaluate the degree of 3D marginal bone remodelling around T3 Prevail implants.

MATERIALS & METHODS:

40 consecutive adult patients, requiring the insertion of dental implants in the aesthetic area (from second premolar to second premolar) will be enrolled in the study. At the time of surgery, a full thickness flap will be elevated, the implant bed will be prepared according to the manufacturer's instruction and the implants will be then seated into the bone. Implants can be placed both with a single-stage or two-stage procedure. Implants inserted with a two-stage procedure will be re-opened after a submerged period of three months.

T0 corresponds to the time of implant insertion, T1 to the time of healing abutment's connection (T0=T1 for single stage implants), and T2 corresponds to 1-year follow-up from healing abutment's connection.

It is supposed that the creation of the biological width starts with the healing abutment's connection.

CBCT scans will be taken immediately after abutment connection (T1) and 1-year after (T2). The midsagittal cut of each implant will be identified, and measurements will be made at predetermined levels. Horizontal facial bone thickness (HFBT) and Vertical facial bone level (VFBL) will be measured. HFBT will be measured at 0, 3, 6 and 9 mm apical to the implant platform. VFBL wil be the perpendicular distance from the implant platform to the most coronal point of the facial bone. Changes between T1 and T2 will be calculated. ;


Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01821092
Study type Interventional
Source Proed
Contact
Status Completed
Phase Phase 4
Start date March 2013
Completion date September 2015

See also
  Status Clinical Trial Phase
Recruiting NCT02880891 - Effects of Splinted or Non-splinted Single-unit Crowns on Marginal Bone-level Alterations Around Implants N/A
Completed NCT00748241 - Study to Evaluate Implant Survival Rate of Astra Tech Fixture ST in the Posterior Maxilla With One-stage Surgery and Early Loading N/A
Active, not recruiting NCT04066309 - Implant Retained Rehabilitation With Surgical and Prosthetic Digital Workflow N/A
Active, not recruiting NCT04545840 - Prospective Neodent® Zirconia System Study
Active, not recruiting NCT06034067 - Osseodensification Versus Conventional Drilling for Implant Site Preparation N/A
Active, not recruiting NCT04546269 - Fully Guided Versus Conventionally Guided Implant Placement by Dental Students N/A
Recruiting NCT02676661 - Evaluation of the Prevalence and Risk Factors for Patients With Peri-implant Disease N/A
Recruiting NCT02662361 - Evaluation of the Prevalence and Risk Factors for Patients With Peri-implant Diseaseļ¼ša Retrospective Study N/A
Completed NCT01030523 - Short Implants - An Alternative to Bone Grafting? N/A
Completed NCT00906425 - Clinical Study Comparing Submerged Versus Trans-mucosal Healing of P.004 Implants in the Anterior Mandible and Maxilla N/A
Completed NCT03252106 - Long-term Effectiveness of Contour Augmentation in Sites With Early Implant Placement N/A
Completed NCT02975674 - Evaluation of MT-12 Implant Survival and Marginal Bone Loss N/A
Completed NCT01822223 - A Study to Evaluate the Effectiveness of Laser-Ablated Implant-Abutments to Promote Tissue Healing N/A
Completed NCT00545818 - Study Comparing OsseoSpeedā„¢ Implants of Two Different Lengths in the Upper and Lower Posterior Jaw N/A
Completed NCT00900822 - Straumann Bone Ceramic Versus BioOss in Sinus Elevation N/A
Completed NCT04017026 - Survival and Success Rates of 6mm Implants With a Micro-rough Surface After 4.5 - 18.2 Years in Function
Active, not recruiting NCT05315414 - Multicenter Study to Evaluate the Clinical Outcome of PrimeTaper EV Implant in Single Tooth Restorations N/A
Recruiting NCT02814149 - Esthetic, Clinical and Radiographic Outcomes of Immediate and Delayed Implant Placement N/A
Active, not recruiting NCT03319758 - Esthetic and Radiographic Outcomes Following Immediate Implant Placement With Thin or Dehiscence Buccal Bone Wall N/A
Completed NCT01807416 - Bone Dimensional Changes at Different Implant-to-abutment Connections: a 1-year Clinical and Radiological Study Phase 4