Dental Restorations

3

Review clinical trials related to Dental Restorations. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Clinical Investigation Measuring the Long Term Clinical Performance and Safety of Biodentine™ XP in Patients Treated for Coronal Restorative or Endodontic Dental Indications.

The aim of this present study is to collect additional data for the post-marketing follow-up of Biodentine™ XP and measure long-term (up to 10 years) performance and safety of the biomaterial in all its indications.

Participants needed: 275
Trial details
Age: 2+Biological sex: AllType: ObservationalSponsor: SeptodontUpdated: May 6, 2026Locations: 8
Eligibility criteria

Temporary tooth, from a child ≥ 2 years old, requiring dental restorative treatm... [+2]

Patient with one or more documented contraindication to use Biodentine™ XP (Refe... [+7]

Status: Not yet recruiting

Sequential Practicing on Psychomotor Skill Acquisition in Undergraduate Dental Students

To determine the influence of hand practice sequence on psychomotor skill acquisition in a glass ceramic onlay preparation among undergraduate dental students.

Participants needed: 28
Trial details
Biological sex: AllType: InterventionalSponsor: Chulalongkorn UniversityUpdated: Apr 2, 2025
Eligibility criteria

The fourth- to sixth-year undergraduate dental students at a single setting of s... [+2]

Status: Not yet recruiting

A Clinical Study Collecting Patients' Experience During Dental Implant Treatment

The study will gather data on patient reported experience (PREM) before, during and after dental implant treatment. Patients scheduled in three treatment groups for either single tooth, multiple teeth or full-arch dental rehabilitation are included in the study and will be treated according standard of care. Additionally, they are asked to report their experience based on pre-defined questionnaire assessing patient acceptance of implant treatment in dentistry. Patients will be followed-up until 1-Year post Final Prosthesis Delivery. This studies primary endpoint is the completion of the PREM questionnaires. The study is not intended to investigate safety and performance of the used medical devices.

Participants needed: 99
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Dr Robert BoweUpdated: Nov 5, 2024
Eligibility criteria

Subject signed informed consent [+6]

Anatomical conditions discovered during surgery preventing the use of intended i... [+6]