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Assessment of the Effects of Different Implant Abutment Occluding Materials on Dental Implant Health Parameters and Microbiology

NCT02625597 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2015-12-09

No results posted yet for this 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

  • Peri-Implantitis
  • Dental Implant Failed
  • Dental Implant Failure Nos

Interventions

DEVICE

Cotton Pellet

DEVICE

Polytetrafluoroethylene Tape

DEVICE

Synthetic Foam

DEVICE

Polyvinylsiloxane

Sponsors & Collaborators

Principal Investigators

  • Julio A Carrion, DMD, PhD · Stony Brook University

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2015-01-31
Completion
2015-06-30

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02625597 on ClinicalTrials.gov