Clinical Performance of Extra-Short (≤5.5 mm) Compared to Longer Implants Splinted under the Same Prosthesis: A Randomized Clinical Trial

Author:

Anitua Eduardo12ORCID,Montalvillo Adriana34,Eguia Asier13,Alkhraisat Mohammad Hamdan125ORCID

Affiliation:

1. University Institute for Regenerative Medicine and Oral Implantology—UIRMI (UPV/EHU-Fundación Eduardo Anitua), 01007 Vitoria, Spain

2. BTI Biotechnology Institute, 01005 Vitoria, Spain

3. Department of Cellular Biology and Histology, Faculty of Medicine and Nursing, Universidad del País Vasco/Euskal Herriko Unibertsitaea (UPV/EHU), 48940 Leioa, Spain

4. Eduardo Anitua Dental Clinic, 01007 Vitoria, Spain

5. Oral and Maxillofacial Surgery, Oral Medicine and Periodontics Department, Faculty of Dentistry, University of Jordan, Amman 11942, Jordan

Abstract

Objective: This randomized controlled split-mouth trial compared the performance of 5.5 mm length implants (test group; TG) splinted within the same fixed prosthesis as longer implants (≥6.5 mm; control group; CG) in posterior regions. Methods: The primary hypothesis was that implant length does not affect marginal bone loss (MBL) one year post-implantation, while the secondary hypotheses included implant survival, peri-implant clinical variables, and prosthetic complications. Fifteen patients (eight males, seven females) with a mean age of 67 ± 9 years were included. Results: No significant difference in the implant position between groups (p = 0.808) was observed. Implant diameters ranged from 3.00 to 4.25 mm, and the most common bone type was type I (67%). Bone density (p = 0.574) and implant insertion torque (p = 0.888) were similar between groups. Mesial MBL (mean: −0.1; range: −1.19 to 0.24 for TG, and −0.03; −1.75 to 0.45 for CG; p = 0.955) and distal MBL (mean: −0.05; range: −1.41 to 0.27 for TG, and 0.08; −1.45 to 0.72 for CG; p = 0.118) did not show statistical differences. There were no implant failures or technical complications. Conclusions: These findings suggest that 5.5 mm length implants could be a viable option for use in posterior regions, providing similar clinical outcomes to longer implants one year post-implantation.

Publisher

MDPI AG

Reference36 articles.

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