bioactive highly filled injectable flowable composite
Otherbioactive highly filled injectable flowable composite
Other names: Shofou Flow Plus X
NCT Number: NCT06790511
The aim of this study is to evaluate Clinical Performance of bioactive highly filled injectable flowable composite for direct posterior occlusal conservative restorations using FDI Criteria
Trial opening soon.
Get Notified16 year–45 year
All sexes
Interventional
Early Phase 1
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
The inclusion criteria: patient age range from 16-45 years, with a premolar indicated for extraction, patients required at least a couple of Class I restorations. The patient should have good general health.
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Exclusion criteria
Where the exclusion criteria will be: poor oral hygiene, sever or chronic periodontal disease or bruxism, severe tooth sensitivity, non-vital or fracture or cracked teeth, defective restorations or bleaching procedures during the last 6 months, pregnancy, and/or lactation, and allergy to the main components of the products to be used in the study.
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bioactive highly filled injectable flowable composite
Other names: Shofou Flow Plus X
highly filled injectable flowable composite
Other names: GC G-ænial Universal Flo
Time frame: 24 Months
Restorations will be assessed for recurrence of caries by visual examination, short air drying
Contact information is provided by the study sponsor or research team.
Cairo University
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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