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DOI: 10.1055/s-0041-1736416
Implant Stability Changes for a Single Implant Mandibular Overdenture
Abstract
Objectives To compare the changes in implant stability for the nonsubmerged and submerged protocols for a single-implant retained mandibular overdenture using Cendres and Metaux Locator attachment throughout a 24-month follow-up.
Materials and Methods Eighty edentulous patients who were seeking to install a single implant in the midline of the completely edentulous mandible. At the day of implant installation, patients were randomized into two groups using sealed envelopes: the nonsubmerged and submerged groups. After 3 months of healing period, randomization using sealed envelopes was performed and patients were randomized to receive the Cendres and Metaux Locator attachment. The periotest readings were recorded using the Periotest M device, every 3 months for the first year and annually in the second year. The scope of this clinical trial focused only on results of the Cendres and Metaux attachment.
Statistical Analysis The Mann–Whitney U-test was used for comparison between study groups for independent samples. Two-sided p-values less than 0.05 were considered statistically significant.
Results There was no statistically significant difference between the mean periotest readings of both groups throughout the 24-month follow-up. Both groups showed an improvement in mean periotest readings with the submerged group tending to show greater stability at 6, 12, and 24-month follow-ups.
Conclusions The nonsubmerged and the submerged healing protocols resulted in reliable periotest readings with the submerged group showing greater improvement than the nonsubmerged, although this improvement is nonsignificant when using the Cendres and Metaux attachment for a single mandibular overdenture.
Authors' Contributions
K.F. was responsible for recording of the periotest values for all groups of patients at the different follow-up intervals throughout the 24-month follow-up. A.F. was responsible for reviewing and editing of the manuscript. Khaled Aziz was responsible for editing the manuscript. M.A.A. was responsible for installing all of the implants. A.N. was responsible for the randomization of patients using sealed envelopes, he was responsible for preparing all of the envelopes and was also responsible for arranging the appointments for the different follow-ups of all recruited patients. N.A.N. was responsible for monitoring all of the clinical steps and interpretation of the data.
Publication History
Article published online:
08 December 2021
© 2021. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
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