Partial-edentulism
Conditions
Brief summary
The main aim of this prospective study is to analyze the survival rate of short-length implants (\<6.5 mm) in subjects with partial edentulism. Non-short length implant will be used as control arm. Additionally, others clinical parameters (marginal bone loss and prosthetic associated complications) will be measured.
Interventions
BTI Dental implants are non-active medical device, single use, non resterilizable, biocompatible and sterile devices made of alloplastic materials (Titanium) intended to be surgically implanted into alveolar and/or basal bone of the mandible or maxilla to provide support and a means of retention for a dental prosthesis (e.g. bridge, single-tooth, overdenture).
Sponsors
Study design
Eligibility
Inclusion criteria
* Age ≥ 18 years * Have planned a fixed multiple prosthesis supported by implants \<6.5 mm in length and implants ≥ 6.5 mm in length within 15 days before the inclusion of the patient in the study. * Planning of supported prostheses from 2 to 4 implants dental * Have a previously performed CBCT (Cone Beam Computed Tomography) * Availability to be observed during the period of tracing * Signature of the informed consent
Exclusion criteria
* Smokers\> 10 cigarettes / day * Complete prostheses * Unitary prostheses
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Survival of dental implants | 1 year | Survival of dental implants at one year post-implantation |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Marginal bone loss | 1 year | Marginal bone loss at one year post-implantation |
| Incidence of prosthetic or implant complications | 1 year | — |
Countries
Spain