Evaluation of the Initial Color Match of Different Single-shade Composites
NCT ID: NCT06473727
Last Updated: 2024-06-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
60 participants
INTERVENTIONAL
2023-05-24
2024-06-16
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Omnichoroma
Anterior non-carious cervical lesions restored with Omnichoroma single-shade resin composite.
Omnichoroma
Patients with anterior non-carious cervical lesions were treated with Omnichoroma. Colour measurements were taken from the middle third of the teeth to be treated using a spectrophotometer. The initial colour measurement was taken from the middle third of the restoration made in the same place and at the same time 24 hours after treatment.
Charisma Topaz One
Anterior non-carious cervical lesions restored with Charisma Topaz One single-shade resin composite.
Charisma Topaz One
Patients with anterior non-carious cervical lesions were treated with Charisma Topaz One. Colour measurements were taken from the middle third of the teeth to be treated using a spectrophotometer. The initial colour measurement was taken from the middle third of the restoration made in the same place and at the same time 24 hours after treatment.
Interventions
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Omnichoroma
Patients with anterior non-carious cervical lesions were treated with Omnichoroma. Colour measurements were taken from the middle third of the teeth to be treated using a spectrophotometer. The initial colour measurement was taken from the middle third of the restoration made in the same place and at the same time 24 hours after treatment.
Charisma Topaz One
Patients with anterior non-carious cervical lesions were treated with Charisma Topaz One. Colour measurements were taken from the middle third of the teeth to be treated using a spectrophotometer. The initial colour measurement was taken from the middle third of the restoration made in the same place and at the same time 24 hours after treatment.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Have healthy gingival tissues
* Presence of an anterior non-carious cervical lesion approximately 5 m wide
Exclusion Criteria
* Signs of fistula
* Pulp exposure
* Periodontal tissue swelling
* Abnormal tooth mobility
18 Years
80 Years
ALL
Yes
Sponsors
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TC Erciyes University
OTHER
Responsible Party
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Ayse Nur Dogan
Lecturer
Principal Investigators
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Ayse Nur Dogan
Role: PRINCIPAL_INVESTIGATOR
TC Erciyes University
Locations
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Faculty of Dentistry, Erciyes University
Kayseri, , Turkey (Türkiye)
Countries
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Other Identifiers
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ErciyesU-DF-AD-01
Identifier Type: -
Identifier Source: org_study_id
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