Clinical Performance of Ceramic Laminate Veneers Made With Celtra Duo

Status Completed

Clinical Trial Summary

The aim of the present study is to assess the clinical performance (patient satisfaction, fracture, shade matching, Marginal adaptation and sensitivity) of laminate veneers made with celtra duo press ceramic and IPS e.max press ceramic with incisal wrap design.

Clinical Trial Description

Ceramic materials are widely used for esthetic restorations because of their physical and optical properties that enhance patient satisfaction to dental restorations. several ceramic materials are currently available, including the lithium-reinforced glass ceramic like e.max press, which stands out for its excellent esthetic appearance and mechanical properties.also ZLS (zirconia-reinforced lithium silicate) are a function of its unique micro structure (500-700 nm in size, correspond exactly to the wavelength range of natural daylight). The presence of 10% zirconia in the glass phase in atomically dissolved form provides high strength and ensures safe and long-lasting restorations .The result is a large number of very fine-grained lithium silicate crystals, whose high glass content give the material its excellent light-optical and mechanical properties. Translucency, opalescence, fluorescence and the chameleon effect all benefit, with high edge stability and excellent polishability being an added plus.3 Despite the recent introduction of improved ceramic materials, patient satisfaction with restoration contour,symmetry,margins and shade matching natural teeth with ceramic restorations is still one of the major challenges in clinical practice. The determination and interpretation of natural tooth color involve the selection and reproduction of ceramic shade and choice of restorative material. These factors have had a major influence on the final color of restorative treatments. Color-measuring instruments assist in shade analysis, thus minimizing the subjective variables of this process. Color readings allow improved determination of the restoration shade and better communication with the dental laboratory.4The influences of underlying substrate,8-9 luting agent,ceramic thickness and translucency, and restoration type14 on the color variation of ceramic restorations have been investigated in in vitro studies. Thus, the purpose of this study was to evaluate clinical performance of celtra duo press ceramic and IPS e.max press ceramic laminate veneers including patient satisfaction, fracture, shad matching, marginal adaptation and sensitivity. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03713970
Study type	Interventional
Source	Cairo University
Contact
Status	Completed
Phase	N/A
Start date	August 25, 2021
Completion date	August 1, 2022

View Details

See also
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	`NCT00115180` - Racial and Ethnic Disparities in Acute Pain Control	N/A
Completed	`NCT00520442` - Acute Pediatric Fracture Analgesia Study	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

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Clinical Performance of Ceramic Laminate Veneers Made With Celtra Duo Press and IPS e.Max Press Ceramic

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms