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XiVE® CAD/CAM Bridges (Abutment-supported/ Implant-supported)

NCT01522365 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2022-09-13

Study results available
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Summary

This study has been designed in order to collect data with regards to the peri-implant tissue outcome of abutment-supported restoration and direct implant-fixed restoration. Therefore a small group of subjects with partly edentulous maxilla is selected to show that both techniques are efficient and safe and to show comparable peri-implant tissue outcome for both methods. At the time of impression forming for each centre treatment A (= abutment-supported XiVE® CAD/CAM supra-structure) and B (= direct implant-fixed XiVE® CAD/CAM supra-structure) is assigned to the left and right side of the maxilla by being randomized at the time of impression forming.

Conditions

  • Partly Edentulous Maxilla

Interventions

DEVICE

Abutment-supported XiVE CAD/CAM bridge

One side will be provided with a XiVE CAD/CAM bridge placed directly on an abutment

DEVICE

Implant-supported XiVE CAD/CAM bridge

One side will be provided with a XiVE CAD/CAM bridge fixed directly on the implant

Sponsors & Collaborators

  • Dentsply Implants Manufacturing GmbH

    lead INDUSTRY

Principal Investigators

  • Manfred Wichmann, Prof. Dr. · Erlangen University Hospital

  • Thomas Dietrich, Prof. Dr. Dr. · Birmingham University, School of Dentistry

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-10-07
Primary Completion
2017-08-08
Completion
2017-08-08

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01522365 on ClinicalTrials.gov