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

NCT ID: NCT02625597

Last Updated: 2015-12-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

8 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-11-30

Study Completion Date

2015-06-30

Brief Summary

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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.

Detailed Description

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Conditions

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Peri-Implantitis Dental Implant Failed Dental Implant Failure Nos

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Dental Materials

Group Type EXPERIMENTAL

Cotton Pellet

Intervention Type DEVICE

Polytetrafluoroethylene Tape

Intervention Type DEVICE

Synthetic Foam

Intervention Type DEVICE

Polyvinylsiloxane

Intervention Type DEVICE

Interventions

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Cotton Pellet

Intervention Type DEVICE

Polytetrafluoroethylene Tape

Intervention Type DEVICE

Synthetic Foam

Intervention Type DEVICE

Polyvinylsiloxane

Intervention Type DEVICE

Other Intervention Names

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Richmond Dental Bleached Cotton Teflon Merco M55 Thread Seal Tape Jordco Endoring Foam Inserts Dentsply Aquasil

Eligibility Criteria

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Inclusion Criteria

* Fully edentulous patient
* Patient has at least one arch restored with a full-arch dental supported prosthesis

Exclusion Criteria

* poor oral hygiene and motivation (as determined with prosthesis in place)
* uncontrolled diabetes
* pregnant or lactating
* substance abusers
* current smokers
* psychiatric problems or unrealistic expectations
* acute infection in the area intended for implant sealing
* positive to HIV and hepatitis B and C
* affected by autoimmune diseases
* under chronic treatment with steroids or non-steroidal anti-inflammatory drugs.
Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Stony Brook University

OTHER

Sponsor Role lead

Responsible Party

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Julio Carrion

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Julio A Carrion, DMD, PhD

Role: PRINCIPAL_INVESTIGATOR

Stony Brook University

Locations

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School of Dental Medicine of Stony Brook University

Stony Brook, New York, United States

Site Status

Countries

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United States

References

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Other Identifiers

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409069

Identifier Type: -

Identifier Source: org_study_id