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Clinical Trial Summary

The purpose of this prospective, open-label, randomized, double arm multicenter study is to evaluate the safety and clinical performance of a newly developed NiTiDent Tuah porous NiTi dental implant (from Nitium Technology Sdn Bhd) in singletooth gap in the posterior mandible 1 year after implant placement and 8 months after implant loading. Second, To investigate the clinical outcome of the interventional dental implant (NiTiDent Tuah Porous NiTi dental implant) compared to control dental implant. The hypothesis is set to no difference in the clinical outcome for the two types of implants based on the outcomes of the primary and secondary endpoints.


Clinical Trial Description

The primary endpoint is to assess implant survival rate over a 12-month period. A surviving implant is defined as an integrated implant in the patient's jaw bone at the time of assessment. Secondary endpoints include the assessment of implant stability, crestal bone levels, peri-implant soft tissue conditions, implant success, and patient satisfaction and related outcomes over several intervals within a 12-month period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04618055
Study type Interventional
Source Nitium Technology Sdn Bhd
Contact Asif A. Khushaini
Phone 60167733360
Email asif@nitiumtech.com
Status Recruiting
Phase N/A
Start date October 15, 2021
Completion date April 15, 2023

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