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One Year Clinical Evaluation of Translucent Zirconia Crowns in Dental Esthetic Zone With Biologically Oriented Preparation Technique (BOPT) Versus Conventional Preparation (Randomized Clinical Trial)

One Year Clinical Evaluation of Translucent Zirconia Crowns in Dental Esthetic Zone With Biologically Oriented Preparation Technique (BOPT) Versus Conventional Preparation (Randomized Clinical Trial)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04320758
Enrollment
22
Registered
2020-03-25
Start date
2020-10-30
Completion date
2020-12-30
Last updated
2020-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Single Crowns in Aesthetic Dental Zone

Brief summary

Aim of the studyto evaluate the clinical behavior of translucent zirconia crown in dental esthetic zone with biologically oriented preparation technique versus conventional preparation.

Interventions

OTHERconventional preparation design

chamfer finish line

shoulder less preparation design

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* All subjects are required to be: 1. From 21-35 years old, be able to read and sign the informed consent document. 2. Have no active periodontal or pulpal diseases, have teeth with good restorations 3. Psychologically and physically able to withstand conventional dental procedures 4. Patients with teeth problems indicated for single all ceramic restoration in maxillary esthetic zone cr 1. Badly decayed teeth 2. Teeth restored with large filling restorations 3. Endodontically treated teeth 4. Malformed teeth 5. Malposed teeth (Tilted, over-erupted, rotated, etc.) 6. Spacing between maxillary teeth in esthetic zone 5. Able to return for follow-up examinations and evaluation

Exclusion criteria

1. Patient less than 21or more than 35 years 2. Patient with active resistant periodontal diseases 3. Patients with poor oral hygiene and uncooperative patients 4. Pregnant women 5. Patients in the growth stage with partially erupted teeth 6. Psychiatric problems or unrealistic expectations 7. Patient with periodontal problems 8. patients with malocclusion or parafunctional habits

Design outcomes

Primary

MeasureTime frameDescription
Marginal adaptation1 yearMeasured using Modified USPHS criteria1

Countries

Egypt

Contacts

Primary ContactKareem Talaat Ali, M>D>s
kareemtalaat@dentistry.cu.edu.eg01002225212
Backup ContactAmina Zaki
aminazaki@dentistry.cu.edu.eg01065550016

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026