Dental Implant, Primary Stability of the Implants
Conditions
Keywords
dental implant, primary implant stability, primary stability, thread design, double thread, triple thread
Brief summary
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
Interventions
DEVICEtriple thread dental implant
Participants 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).
DEVICEdouble thread dental implant
Participants 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).
Sponsors
Future University in Egypt
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)
Masking description
Participants will be blinded to the type of implant thread design received. The investigator will not be blinded because the investigator performs the implant placement and measures implant stability.
Intervention model description
participants will be randomly assigned to two parallel groups. One group will receive double-thread dental implants, while the other group will receive triple-thread dental implants. Primary implant stability will be compared between the two groups
Eligibility
Sex/Gender
ALL
Age
20 Years to 55 Years
Healthy volunteers
No
Inclusion criteria
* 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. * Signed informed consent for participation in the study.
Exclusion criteria
* 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. * Individuals with a history of allergic reactions to implant materials.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| insertion torque | at the time of implant placement T0 | 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
| Measure | Time frame | Description |
|---|---|---|
| implant stability (ISQ) | 3 months | 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 |
Contacts
CONTACTfalah M Alshahrani, BDS
Outcome results
None listed