A Comparative Study to Evaluate Bone Height Gain Following Transcrestal Sinus Floor Elevation Using Specially Designed Drills Versus the Conventional Osteotome Technique.
Status
Conditions
Treatments
Details and patient eligibility
About
Radiographic evaluation of the amount of bone height gain and clinical evaluation of the possibility of developing complications after transcrestal sinus floor elevation using drills and the conventional osteotome technique.
Full description
Short implants (< 10 mm) are one of the options used to overcome low vertical bone height in the maxilla. However, short implants have faced many challenges as smaller implant surface; therefore less bone-to-implant contact after osseointegration with force distribution on a reduced surface after loading. This leads to more crestal bone resorption with more threads exposure decreasing the long term implant success Another treatment option is placing implants in specific anatomical areas, such as the pterygoid region or the zygoma .Many complications are reported as postoperative sinusitis, temporary paresthesia, epistaxis, facial, periorbital hematoma, orbital penetration and prosthetic difficulties due to the implants palatal emergence.
Vertical augmentation with bone grafts is another treatment option. However, it has many drawbacks as the unpredictable graft resorption, low bone to implant contact, higher possibility of wound dehiscence, as well as compromised implant position leading to undesirable prosthetic restorations.
To overcome the problems of the previously mentioned procedures, elevation of the sinus membrane techniques were proposed, it can be performed either through a lateral window , or via a crestal access depending on the remaining bone height (RBH). If the RBH is around 6-9 mm, the crestal approach is indicated. If the RBH is less than 5 mm, a lateral approach should be performed.
For the crestal approach, it could be performed by the conventional osteotome technique. However, it is a visually restrictive technique which may lead to sinus perforation as well as it can cause some complications as headache and paroxysmal positional vertigo (Saker e Ogle, 2005; Peñarrocha-Diago et al., 2008).
To overcome the disadvantages of the conventional osteotome technique, various kits have been developed for transcrestal sinus floor elevations using specially designed drills.
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
Inclusion criteria
Patients having at least one missing upper posterior tooth.
Residual bone height beneath maxillary sinus from 5-8 mm .
A minimum of 6 mm residual bone width.
The recipient site of the implant should be free from any pathological condition.
No diagnosed bone disease or medication known to affect bone metabolism.
Patients who are cooperative, motivated and hygiene conscious.
Patients having proper inter-occlusal space.
Exclusion criteria
Systemic conditions/disease that contraindicated surgery.
Radiation therapy in the head and neck region or chemotherapy during the 12 months prior to surgery.
Patients who have any habits that might jeopardize the osseointegration process, such as current smokers.
Patients with parafunctional habits that produce overload on implant, such as bruxism and clenching.
Patients that have any pathology in the maxillary sinuses.
Trial design
Primary purpose
Allocation
Interventional model
Masking
18 participants in 2 patient groups
Trial contacts and locations
Loading...
Central trial contact
Omar A Ashour, Bachelor
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal