Alveolar Bone Loss
Conditions
Brief summary
Recently, 4 mm long implants with a standard diameter have been used for the restoration of the posterior edentulous mandible with favorable results. However, randomized clinical trials reporting the results from full-arch fixed dental prosthesis that included 4 mm long implants placed in the posterior regions of the maxilla have not been published yet. The aim of the present study will be to compare the survival and success rates of 4 mm implants used as distal support of a maxillary full-arch fixed dental prosthesis with standard (10 mm) implants placed in association with a bilateral sinus floor augmentation procedure
Detailed description
Two groups will be randomly prepared, the Short group and the Standard group. In the Short group, one 4 mm long and 4.1 mm in diameter implant (extra-short implant) will be installed in each side of the posterior region of the maxilla. In the Standard group, bilateral sinus floor elevations will be performed. After 4 months of healing, one 10 mm long and 4.1 mm in diameter implant (standard implant) will be installed into each augmented sinus. In the frontal region, four 10 mm long implants will be installed in both groups. Clinical assessments and x-rays will be taken at prosthesis delivering (6-8 weeks after implant installation), and after 6, 12, 18 and 24 months.
Interventions
PROCEDUREPlacement of extra short implants
placement of an extra short implant in the posterior edentulous ridge
PROCEDUREmaxillary sinus lift, maxillary sinus elevation, maxillary sinus augmentation
PROCEDUREplacement of standard implant
placement of standard implant in the posterior edentulous ridge after maxillary sinus augmentation
Sponsors
University of Bologna
ITI International Team for Implantology, Switzerland
ARDEC Academy
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)
Masking description
A statistician not involved in the study performed the randomization in blocks of four and the assignments have been sealed in coded and opaque envelopes that will be opened at the time of the enrollment of each patient in the study. The surgeon will be blinded about the assignment until the time of the surgery. The outcome assessor will be blinded about the protocol
Intervention model description
Two groups will be randomly prepared. The Short group, one 4 mm long and 4.1 mm in diameter implant (Short implant) will be installed in each side of the posterior region of the maxilla. The standard group, bilateral sinus floor elevations will be performed. After 4 months of healing, one 10 mm long and 4.1 mm in diameter implant (Standard implant) will be installed into each augmented sinus.
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes
Inclusion criteria
* Edentulous maxilla * Willing to receive a full arch fixed restoration in the maxilla. * Latest extraction at least 8 weeks before implant insertion * Sinus floor height included between 4 to 6 mm * Bone width in the distal segments sufficient to allow the insertion of a 4 mm long implant of standard diameter. * In the anterior maxilla (from first premolar to first premolar) bone width sufficient to allow the insertion of 10 mm long implants of standard diameter. Minor horizontal augmentations with guided bone regeneration procedures was allowed in the anterior maxilla. the opposing arch have to present one of the following conditions: * natural dentition (at least 10 elements from 3.5 to 4.5) * Fixed dental prosthesis of at least 10 elements (from 3.5 to 4.5) supported by teeth or implants * Implant supported or teeth supported overdentures * Adequate partial removable prostheses.
Exclusion criteria
* Presence of conditions requiring prophylactic use of antibiotics (e.g., history of rheumatic heart disease, bacterial endocarditis, cardiac valvular anomalies, prosthetic joint replacements). * Major systemic diseases, or medical conditions requiring prolonged use of steroids, or alcoholism or chronically drug abuse. * Current pregnancy or breastfeeding women * Smokers \> 10 cigarettes per day * Physical handicaps that would interfere with the ability to perform adequate oral hygiene * Immunocompromised patients including patients infected with HIV * Conditions or circumstances, in the opinion of the investigator, which would prevent completion of study participation or interfere with analysis of study results, such as history of non-compliance, or unreliability. * Patients with an ongoing or previous treatment with bisphosphonates (for at least 2 months for oral therapy or 6 months for IV injection) Local
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| survival rate of 4 mm implants used as distal support | 24 months | To compare the survival rates of 4 mm implants used as distal support of a maxillary full-arch fixed dental prosthesis with standard (10 mm) implants placed in association with a bilateral sinus floor augmentation procedure. |
| Crestal bone level | 24 months | Change of crestal bone level measured on intraoral x-ray applying a parallel technique from baseline (definitive prosthesis delivering) and 2-year follow-up. The distance between the implant margin and the first bone to implant contact will be measured in millimeters at the mesial and distal aspects of the Short and Standard implants. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Technical complications | 24 months | Any technical complications related to implants, abutments, screw loosening, prosthetic fracture or chipping of the veneer material expressed in number of occurrence. |
Outcome results
None listed