Objectives
To conduct a randomised controlled trial to evaluate the shortâterm clinical and radiographic efficacy of the NobelActiveâą system and to evaluate the relative importance of achieving primary stability at placement.
Materials and methods
A total of 32 subjects were recruited and, using a splitâmouth design, the NobelActiveTM implant was compared with a contralaterally matched BrĂ„nemark implant. Both implants were placed in a single surgical procedure into healed sites using a oneâstage protocol and reviewed at monthly intervals. NobelActiveTM implants were functionally loaded with provisional restorations at 1 month and all implants were restored with final crowns 3 months postâimplant placement. The implant was assessed using peak insertion torque values, resonance frequency analysis (RFA), clinical parameters, digital subtraction radiography, and cone beam computed tomography.
Results
The insertion torque was significantly greater for the NobelActiveTM implant group (PÂ =Â 0.02), although no observable difference in RFA values were found. Preliminary results of 6Â months followâup suggest comparable clinical and radiographic healing responses between the test and control implants. Within the limits of the sample population, the survival rates were lower with the test implants, although this difference was not statistically significant.
Conclusions
The NobelActiveTM implant system requires higher insertion torques and can also achieve greater primary stability compared with a control implant system. Shortâterm survival and marginal bone levels of NobelActiveTM and control implants are comparable, although the NobelActiveTM implant system appeared to be more techniqueâsensitive.