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NCT05751382

Evaluation of Self-adhesive Hybrid Resin Composite Compared to a Traditional Composite Resin in Restorations of NCCLs

Terminated NA Results posted Last updated 13 January 2025
What this trial tests

NA trial testing Surefil one in Tooth Restoration in 16 participants. Terminated before completion.

Timeline
21 September 2022
Primary endpoint
22 January 2024
22 January 2024

Quick facts

Lead sponsorDentsply Sirona Implants and Consumables
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment16
Start date21 September 2022
Primary completion22 January 2024
Estimated completion22 January 2024
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Dentsply Sirona Implants and Consumables — full company profile →

Who can join

Adults 18 to 70, any sex, with Tooth Restoration. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a split-mouth randomized clinical investigation conducted to evaluate clinical performances of a self-adhesive hybrid resin composite (investigational medical device Surefil) compared to a traditional composite resin, when used for direct restorations of non-carious lesions (NCCLs). The study consists of a 3-year long follow-up period.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Tooth Restoration

Currently open trials in the same condition.

Other Dentsply Sirona Implants and Consumables trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05751382.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing