Skip to main content
Clinical Trials/NCT03779607
NCT03779607UnknownNot Applicable

Clinical Evaluation and Patient Satisfaction Ofshade Matching Between Natural Teeth and Monolithic All-ceramic Crowns Fabricated From Two Materials (Randomized Controlled Clinical Trial)

Cairo University0 sites10 target enrollmentStarted: January 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
10
Primary Endpoint
Color match

Study Overview

Brief Summary

evaluation of color difference between zirconia reinforced lithium silicate (celtra press) VS lithium disilicate (Emax) in relation to natural tooth structure to determine which monolithic material will provide restoration with exact shade and optical properties as natural tooth structure.

Detailed Description

eligible patients will be randomized in 2 equal group between study group (celtra press) and control group (Emax) .

Single tooth in esthetic zone requiring full coverage crown is prepared to receive an all ceramic crown of .

Grouping: The crowns will be divided into two groups:

I:Teeth receiving crowns fabricated from IPS emax press ( ivoclarvivadent) II:Teeth receiving crowns fabricatedfrom Celtrapress(dentsplysirona).

Shade will be measured using intraoral spectrophotometer and evaluated.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
20 Years to 45 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age range of the patients from 20-45 years old; able to read and sign the informed consent document, illiterate patient will be avoided.
  • Patients able physically and psychologically to tolerate conventional restorative procedures.
  • Patients with no active periodontal or pulpal diseases, having teeth with good restorations.
  • Patients with teeth problems indicated for full coverage restoration ( coronal fracture where partial coverage would lack retention, malposed or malformed teeth).
  • Patients with root canal treated teeth requiring full coverage restorations with contralatral tooth not filled orfractured.
  • Patients willing to return for follow-up examinations and evaluation.

Exclusion Criteria

  • Patients in the growth stage with partially erupted teeth.
  • Patients with poor oral hygiene and motivation.
  • Pregnant women's to avoid any complication that may occur in dental office due to pregnancy or due to injected anesthetic solution.
  • Patients with psychiatric problems or unrealistic expectation
  • Patients have no opposite occluding dentition in the area intended for restoration\
  • Patients suffer from parafunctional habits.
  • deep discoloration of abutment .
  • Smokers and heavy caffeine consumers.

Outcomes

Primary Outcomes

Color match

Time Frame: immediately after crown cementation

using USPHS scoring system

Secondary Outcomes

  • Patient satisfaction(immediately after crown cementation)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mohamed el sayed bekhiet

Resident - Fixed prosthodontic department- Faculty of oral and dental medicine

Cairo University

Similar Trials