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NCT02625597 · ClinicalTrials.gov registry record · NA
Assessment of the Effects of Different Implant Abutment Occluding Materials on Dental Implant Health Parameters and Microbiology
A NA study of Peri Implantitis and Dental Implant Failed, sponsored by Stony Brook University.
- Completed
- Registry status
- NA
- Development phase
- 8
- Enrollment target
- 1
- Study location
NCT02625597: Completed NA study of Peri Implantitis and Dental Implant Failed, sponsored by Stony Brook University.
NCT02625597 is a NA study of Peri Implantitis and Dental Implant Failed that has completed, run by Stony Brook University. The registered enrollment target is 8 participants, below the 118-participant average among 4 other Peri Implantitis trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02625597, a NA study of Peri Implantitis and Dental Implant Failed, has completed, sponsored by Stony Brook University.
- COMPLETED
- Registry status
- NA
- Development phase
- 8 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary purpose of this study is to determine what effect, if any, do different dental materials used to seal the prosthetic screw channels of implant supported restorations have on dental implant health parameters and microbiology.
Conditions Studied
Interventions
- DEVICE Cotton Pellet
- DEVICE Polytetrafluoroethylene Tape
- DEVICE Synthetic Foam
- DEVICE Polyvinylsiloxane
Study Locations (1)
New York
- School of Dental Medicine of Stony Brook University - Stony Brook
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 8 participants |
| Start Date | 2013-11 |
| Est. Completion | 2015-06 |
| Phase | NA |
What the finished NCT02625597 record still lists
NCT02625597 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 118-participant average among 4 other Peri Implantitis trials with a reported enrollment target (93% lower).
The record links to 3 conditions, with Peri Implantitis appearing as the primary indexed condition, and to 4 interventions - of which Cotton Pellet is the first listed.
NCT02625597 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT02625597 about?
NCT02625597 is a clinical study titled "Assessment of the Effects of Different Implant Abutment Occluding Materials on Dental Implant Health Parameters and Microbiology". The primary purpose of this study is to determine what effect, if any, do different dental materials used to seal the prosthetic screw channels of implant supported restorations have on dental implant health parameters and microbiology.
What is the current status of trial NCT02625597?
This trial is currently completed. It is a NA study. The enrollment target is 8 participants. The study started on 2013-11. Estimated completion is 2015-06.
What conditions does trial NCT02625597 study?
This clinical trial studies the following conditions: Peri Implantitis, Dental Implant Failed, Dental Implant Failure Nos.
What interventions are being tested in trial NCT02625597?
The interventions under investigation include: Cotton Pellet (DEVICE), Polytetrafluoroethylene Tape (DEVICE), Synthetic Foam (DEVICE), Polyvinylsiloxane (DEVICE).
Who is sponsoring clinical trial NCT02625597?
This trial is sponsored by Stony Brook University, which has 127 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02625597 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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