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NCT04708223 · ClinicalTrials.gov registry record · NA
Prospective, Split-mouth, Comparative Study to Compare Clinical Outcomes of Two Different Posterior Composite
A NA study, sponsored by Ivoclar Vivadent.
- Completed
- Registry status
- NA
- Development phase
- 51
- Enrollment target
NCT04708223 is a NA study that has completed, run by Ivoclar Vivadent. The registered enrollment target is 51 participants.
The verdict
NCT04708223, a NA study, has completed, sponsored by Ivoclar Vivadent.
- COMPLETED
- Registry status
- NA
- Development phase
- 51 participants
- Enrollment target
Study Summary
The objective of this 2-year split mouth comparative study, a randomized controlled study, is to determine whether the simplified placement procedure of the ultra-rapid polymerizing Tetric PowerFlow/ Tetric PowerFill with a reduced light polymerization time (3 s), yields the same clin-ical results as widely used commercially available dental composites (Tetric EvoCeram Bulk Fill, Tetric EvoFlow Bulk Fill) requiring up to 40 seconds of light polymerization time.
Interventions
- DEVICE Direct restorative treatment with fast-curing composites (Tetric PowerFill/ Tetric PowerFlow)
- DEVICE Direct restorative treatment with conventionally applied composites (Tetric EvoCeram Bulk Fill/ Tetric EvoFlow Bulk Fill)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 51 participants |
| Start Date | 2018-09-01 |
| Est. Completion | 2022-05-16 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04708223
The ClinicalTrials.gov registry entry for NCT04708223 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 51 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ivoclar Vivadent, which has 4 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Direct restorative treatment with fast-curing composites (Tetric PowerFill/ Tetric PowerFlow) is the first listed.
NCT04708223 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04708223 about?
NCT04708223 is a clinical study titled "Prospective, Split-mouth, Comparative Study to Compare Clinical Outcomes of Two Different Posterior Composite". The objective of this 2-year split mouth comparative study, a randomized controlled study, is to determine whether the simplified placement procedure of the ultra-rapid polymerizing Tetric PowerFlow/ Tetric PowerFill with a reduced light polymerization time (3 s), yields the same clin-ical results a...
What is the current status of trial NCT04708223?
This trial is currently completed. It is a NA study. The enrollment target is 51 participants. The study started on 2018-09-01. Estimated completion is 2022-05-16.
What interventions are being tested in trial NCT04708223?
The interventions under investigation include: Direct restorative treatment with fast-curing composites (Tetric PowerFill/ Tetric PowerFlow) (DEVICE), Direct restorative treatment with conventionally applied composites (Tetric EvoCeram Bulk Fill/ Tetric EvoFlow Bulk Fill) (DEVICE).
Who is sponsoring clinical trial NCT04708223?
This trial is sponsored by Ivoclar Vivadent, which has 4 total clinical trials registered on ClinicalTrials.gov.
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