Clinical Trials Directory

Trials / Completed

CompletedNCT05712031

Combined Tooth-implant Supported Prostheses

Clinical Evaluation of Combined Tooth-implant Supported Prosthesis: Controlled Prospective Clinical Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
78 (actual)
Sponsor
ORHUN EKREN · Academic / Other
Sex
All
Age
37 Years – 73 Years
Healthy volunteers
Accepted

Summary

The goal of this clinical study is to evaluate clinical performance of combined tooth-implant supported 3 unit fixed partial dentures in the posterior mandible and was to compare and evaluate them with the complications of 3 unit fixed partial dentures supported with free standing dental implants.The main question\[s\] it aims to answer are: 1.Is there any difference in terms of mechanical and biological complications as well as marginal bone level between free standing and combined tooth-implant supported 3 unit Fixed Partial Dentures in posterior mandible. Participants will receive either 2 dental implants(Control group) or 1 standart length dental implants to be combine with abutment tooth or 1 short dental implant to be combine with abutment tooth for supporting 3 unit fixed partial dentures.

Detailed description

Purpose: The aim of the study was to evaluate clinical performance of combined tooth-implant supported 3 unit fixed partial dentures in the posterior mandible and was to compare and evaluate them with the complications of 3 unit fixed partial dentures supported with free standing dental implants. Material and methods: 78 partially edentulous patients in the posterior mandible (Kennedy 1 and Kennedy 2), age between 18-65 with no systemic disorders were recruited for the study (n=26). Group 1served as control group and received 2 dental implants for supporting 3 unit fixed partial dentures (FPD). In group 2 dental implants longer than 8 mm and in group 3 shorter than 8 mm were inserted to replace first or second molar combined with first or second premolar respectively to support cement retained 3 units FPD. Periapical radiographs were taken with parallel technique for evaluation of marginal bone resorption (CBL) and modified plaque index (MPI), bleeding index (BI) and sulcus depth of abutment teeth was recorded at the time of FPD insertion, 6 months after FPD insertion and annually. Abutment tooth intrusions, de-cementation of the restoration, porcelain chipping/delamination, framework fracture, abutment screw loosening, abutment and abutment screw fracture, implant fracture were also recorded as complications.

Conditions

Interventions

TypeNameDescription
PROCEDUREInsertion of 1 Nucleoss T4 dental implants in posterior mandibleNucleoss T4 dental implants is combined with first or second premolar to support 3 unit fixed partial dentures
PROCEDUREInsertion of 1 Nucleoss T5 dental implants in posterior mandibleNucleoss T5 dental implants is combined with first or second premolar to support 3 unit fixed partial dentures
PROCEDUREInsertion of 2 Nucleoss T4 dental implants posterior mandible2 freestanding Nucleoss T4 dental implants is used to support 3 unit fixed partial dentures

Timeline

Start date
2015-07-03
Primary completion
2022-06-06
Completion
2022-09-09
First posted
2023-02-03
Last updated
2023-02-03

Source: ClinicalTrials.gov record NCT05712031. Inclusion in this directory is not an endorsement.