Fracture Clinical Trial
Official title:
Randomized Controlled Clinical Trial to Compare Posterior Implant-Supported Modified Monolithic Zirconia and Metal-Ceramic Single Crowns: 5 Years Study
The outcome of implant therapy has been presented in the majority of clinical studies by
focusing only on implant survival without providing detailed information on the
reconstructions . However, for decision making, it is important to know the survival rates
and the incidence of biological and technical complications not only for the implants but
also for the reconstructions. Thus, the selection of restoration materials should be based on
proper optical characteristics in addition to biocompatibility and sufficient strength of
materials.
Monolithic zirconia has been used in posterior region, especially for single crowns, in order
to eliminate the veneer cracking, But Since monolithic zirconia are relatively new, few
randomized, controlled clinical studies have evaluated their success. There is only one study
identified regarding the performance of monolithic ceramic restorations bonded to Ti inserts,
investigating the clinical outcome of using monolithic or modified monolithic zirconia
implant-supported single crowns and comparing outcomes and complications of metal-ceramic and
monolithic or modified monolithic zirconia implant supported single crowns.
More clinical studies to evaluate the performance of CAD/CAM monolithic implant-supported
restorations bonded to Ti inserts and bases and compare their survival, success and
complication rates with other restorative options [with a mean follow-up period of at least 5
years are required for a meaningful interpretation of the survival and complication rate .
So this study aims to investigate outcomes and complications of implant supported modified
monolithic zirconia and metal-ceramic single crowns in the posterior region of the mouth.
The null hypothesis is that there is no difference between modified monolithic zirconia and
metal-ceramic posterior implant-supported SCs in prosthetic complication rates.
Background: Dental implants restored with single crowns (SCs) have been reported to have a
comparable survival rate and fewer technical complications compared to multiple-unit
implant-supported FDPs. Porcelain-fused to metal restorations were the golden standard option
for implant supported reconstructions in the past, but nowadays, the application of
all-ceramic restorations in general and specifically zirconia as a restorative material for
implant-supported single crowns has increased utilizing the CAD/CAM technology. The
continuous technological progress in both the computer-based development and the dental
manufacturing process ensures new opportunities in the clinical workflow. A fully digital
pathway in a model-free approach or a combination of these workflows is now possible.
Purpose: The purpose of this randomized controlled clinical trial is to investigate the
prosthetic outcomes of posterior implant-supported single crowns (SCs) with a modified
monolithic zirconia or metal-ceramic design utilizing the digital workflow at 1, 3 and 5
years of loading.
Materials and methods: This single-blind split mouth study will enroll 60 participants,
having to receive 120 dental Implants. They will be scheduled for a bilateral posterior
single-unit prosthetic rehabilitation supported by one implant in the posterior region of the
maxilla or the mandible (premolars, molars). A fully digital pathway will be followed. A CT
scan will be performed without any template. An intraoral optical impression using CEREC
Omnicam scanner will be made. A virtual set-up of the prosthetic reconstruction, as well as a
surgical template with optimal 3-D implant positioning will be designed then printed using a
3-D printer without the need of any physical model. Straumann bone level implants with either
a wide diameter (Ø4.8 mm) or regular diameter (Ø4.1 mm) with a minimum length of 8 mm will be
inserted. Implants will be loaded after 3 months of submerged healing. A second intraoral
optical impression will be made using CEREC Omnicam scanner and Straumann scanbody. The
implant-supported prosthetic suprastructure will be designed. Implants will be randomly
allocated to either the test group modified monolithic zirconia crowns (MMZ) or the control
group metal ceramic crowns (MC), using a computer-generated randomization list. A digital
model with movable dies will be 3-D printed, then used to adjust restoration in terms of
occlusal and proximal contacts. Prefabricated screw-retained Titanium abutments (Variobase
Abutment; Straumann) will be used as the metal substructures of the crowns and will be
secured to lab analogues on the digitally printed casts. Metal/ zirconia substructures with a
hole for the screw retention will be designed using the CAD software and will be anatomically
reduced by 1 mm to allow for porcelain veneering then will be laser-printed/ dry milled. Hand
layering of glass ceramic will be made on the surface. Crowns will be cemented extraorally to
titanium abutments using dual cure resin cement to make one-piece screw-retained single
crown. The screw-retained single crowns and titanium abutments will be inserted intraorally
with 35 Ncm torque and screw-access holes will be restored with Teflon and light-polymerized
composite resin. The implant-supported SCs will be examined after 1, 3 and 5 years for
survival and technical complications.
Clinical significance: to evaluate the survival and prosthetic complication rates of
zirconia-ceramic and metal-ceramic implant-supported single crowns at 1, 3 and 5 years of
service. In addition to that, the digital workflow for implant supported single crowns will
be evaluated for efficiency, accuracy, time and cost compared to conventional workflow.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Withdrawn |
NCT04470895 -
Impact of Drugs on the Risk of Falls in the Fracture Department of the Paris Saint-Joseph Hospital Group
|
||
Recruiting |
NCT02635022 -
Fragility Fracture Liaison Service and Anti-osteoporosis Medication Monitoring Service Study
|
||
Unknown status |
NCT02013986 -
Effects of Etomidate on Postoperative Circadian Rhythm Changes of Salivary Cortisol in Children
|
Phase 4 | |
Terminated |
NCT01248182 -
Bone to Skin Thickness Study: Obese Versus Normal Population
|
N/A | |
Recruiting |
NCT00969839 -
NovaLign Intramedullary Fixation System (IFS) for the Treatment of Humeral Fractures
|
Phase 4 | |
Completed |
NCT00520442 -
Acute Pediatric Fracture Analgesia Study
|
N/A | |
Completed |
NCT00115180 -
Racial and Ethnic Disparities in Acute Pain Control
|
N/A | |
Not yet recruiting |
NCT06402292 -
Surgical Treatment of Osteoarticular Infections Using Bioactive Bone Substitute
|
N/A | |
Recruiting |
NCT04947722 -
The PREVENT Trial: a Pragmatic Cluster Randomized Controlled Trial of a Multifaceted Fracture Prevention Model for Long-term Care
|
N/A | |
Recruiting |
NCT06107699 -
The CHARM Study-Coordinating Transitions From Hospital for Older Adults With Fractures
|
N/A | |
Completed |
NCT04532580 -
Clinical Validation of Boneview for FDA Submission
|
||
Completed |
NCT04237454 -
Thermal Imaging Compared to Skeletal Survey in Children Below 2 Years
|
N/A | |
Recruiting |
NCT05002335 -
Clinical and Radiological Outcomes of Medacta Shoulder System (BE)
|
||
Completed |
NCT02591043 -
Surgical Treatment of Low Energy Pelvic Fractures in the Elderly
|
N/A | |
Completed |
NCT02933359 -
Osteogenic Profiling of Normal Calvarial Bone
|
||
Completed |
NCT01049191 -
Bone Microarchitecture in Women With and Without Fracture
|
N/A | |
Completed |
NCT03431857 -
Multi Centre Study on TESS V2 Shoulder System
|
||
Recruiting |
NCT04133103 -
Early Mobilisation in the Surgical Robot Assisted Spinal Surgery
|
N/A | |
Completed |
NCT03993691 -
Wrist Fracture Evaluation With a Desktop Orthopedic Tomosynthesis System
|
N/A | |
Active, not recruiting |
NCT01719887 -
Effectiveness and Cost-effectiveness of Surgical Treatment of Humeral Shaft Fractures. Randomized Controlled Trial
|
N/A |