U.S., Oct. 8 -- ClinicalTrials.gov registry received information related to the study (NCT07862218) titled 'Accuracy of Complete-Arch Implant Scans Using Non Calibrated Splinting Scanbodies' on Oct. 01.
Brief Summary: This randomized crossover clinical study will evaluate and compare the accuracy and chairside time of two non-calibrated splinting systems, IoConnect and Scan Pro, for obtaining complete-arch implant digital scans. The study will include completely edentulous patients with four well-integrated implants connected to multiunit abutments.
Each participant will undergo complete-arch implant scanning using both systems, with the order of the scanning protocols determined by a computer-generated randomization sequence. The digital...