About this trial
The goal of this randomized clinical trial is to compare the primary stability of double-thread and triple-thread dental implant designs in patients requiring implant placement in the posterior maxilla.
The main question it aims to answer is whether implant thread design influences primary implant stability in the posterior maxilla.
Participants will be randomly assigned to one of two groups. Group A will receive a double-thread dental implant, while Group B will receive a triple-thread dental implant. Primary implant stability will be assessed at the time of implant placement using insertion torque and resonance frequency analysis (ISQ).implant stability using ISQ will also be evaluated at 3 months
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients aged 20-55 years.
Medically healthy individuals without any systemic disease that affects bone healing (e.g., uncontrolled diabetes, osteoporosis).
Patients requiring dental implants in the posterior maxilla.
Adequate bone volume for implant placement.
Disqualifiers
Smokers (due to the potential negative impact on bone healing and implant success).
Pregnant or breastfeeding women.
Patients with a history of radiotherapy or chemotherapy.
Patients with severe periodontal disease.
Trial design
Parallel
Treatments tested in this trial
triple thread dental implant
DeviceParticipants assigned to this group will receive a triple-thread dental implant placed in the posterior maxilla. Primary implant stability will be assessed at the time of implant placement using insertion torque and resonance frequency analysis (ISQ).
double thread dental implant
DeviceParticipants assigned to this group will receive a double-thread dental implant placed in the posterior maxilla. Primary implant stability will be assessed at the time of implant placement using insertion torque and resonance frequency analysis (ISQ).
Treatment groups
Trial outcomes
Primary outcomes
insertion torque
The primary outcome of this study will be the insertion torque, expressed in Newton-centimeter (Ncm). Measurements will be performed using a surgical motor/torque wrench and recorded at the time of implant placement (T0).
Secondary outcomes
implant stability (ISQ)
The first secondary outcome will be the assessment of implant stability (ISQ) using the Osstell ISQ device. The measurements will be expressed on the ISQ scale (1-100) and recorded at the time of implant placement (T0). The second secondary outcome will also be the evaluation of implant stability (ISQ), assessed with the Osstell ISQ device on the ISQ scale (1-100), but recorded at 3 months, corresponding to the prosthetic stage
Locations
Sponsors and contacts
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