Straumann Bone Ceramic Versus BioOss in Sinus Elevation

Straumann

Status

Completed

Conditions

Jaw, Edentulous, Partially

Alveolar Bone Loss

Treatments

Device: BioOss

Device: Straumann Bone Ceramic

Study type

Interventional

Funder types

Industry

Identifiers

NCT00900822

CR 02/05

Details and patient eligibility

About

Straumann Bone Ceramic (SBC) and BioOss will be used as bone grafting materials when there is a need for bone augmentation in the posterior upper jaw. 9 months later the bone formation is evaluated. The patients are followed for 3 years.The study hypothesis is that the SBC is not worse than BioOss.

Full description

Straumann Bone Ceramic (SBC) and BioOss will be used as bone grafting materials when there is a need for bone augmentation in the posterior upper jaw. The bone grafting materials will be placed into the sinus cavity,(a routine procedure), one material randomly at each side and a micro-implant will be inserted simultaneously. 9 months later the micro-implant is removed and a regular Straumann SLActive implant is inserted. The micro-implant is evaluated histologically. The site is evaluated every 12 months for 3 years in regards to clinical measurements. The study hypothesis is that the SBC is not worse than BioOss.

Study design: Prospective, randomized, open, controlled, single center, split mouth

Study population: 11 male and female patients at an age of between 18 and 80 years, affected by edentulism of both lateral-posterior maxilla and presenting two pneumatized maxillary sinuses and necessitating rehabilitation with implant-supported prostheses will be recruited in the study and treated by means of maxillary sinus floor augmentation and delayed implant placement.

Enrollment

11 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Males and females, 18 years to 80 years of age
The patients are at least partly edentulous in the both maxillary regions corresponding to the sinuses.
A dental implant procedure is foreseen in both maxilla regions corresponding to maxillary sinuses.
Patients must be expected to present a bilateral bone defect in the sinus area, which both need a sinus floor augmentation to place one or more dental implants each.
Residual alveolar crest height of the lateral-posterior segments of the edentulous maxilla below the floor of each of the maxillary sinuses shall be
less than 5 mm and at least 2 mm, as measured by Scanora - tomography Scans in the deepest floor of the sinus
residual alveolar crest width should be at least in average more than 4mm as measured by Scanora - tomography scans
Patients must be committed to the study and must sign informed consent.
Oral hygiene Index less than 25%

Exclusion criteria

Any systemic medical condition that could interfere with the surgical procedure or planned treatment
Current pregnancy at the time of recruitment
Physical handicaps that would interfere with the ability to perform adequate oral hygiene
Alcoholism or chronically drug abuse causing systemic compromize
Patients who smoke more than 10 cigarettes per day
Medication which interferes with bone formation
Conditions or circumstances, in the opinion of the investigator, which could represent a general contra-indication for surgical procedure or would prevent completion of study participation or interfere with analysis of study results, such as history of non-compliance, or unreliability
Mucosal diseases such as erosive lichen planus
History of local radiation therapy
Presence of oral lesions (such as ulceration, malignancy)
Severe bruxing or clenching habits
Persistent intraoral infection
Previous GBR (bone graft) or dental implant treatment in the posterior segments of the upper maxilla (foreseen implant site)
Patients presenting clinical and radiological signs and symptoms of maxillary sinus disease
Existing teeth in the residual dentition with untreated endodontic problems