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

An In Vivo Assessment of the Effects of Using Different Implant Abutment Occluding Materials on Implant Microleakage and the Peri-Implant Microbiome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02625597
Enrollment
8
Registered
2015-12-09
Start date
2013-11-30
Completion date
2015-06-30
Last updated
2015-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Brief 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.

Interventions

DEVICECotton Pellet
DEVICEPolytetrafluoroethylene Tape
DEVICESynthetic Foam
DEVICEPolyvinylsiloxane

Sponsors

Stony Brook University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frame
Probing Depth6 months

Secondary

MeasureTime frame
Gingival Index6 Months
Plaque Index6 Months
Microbial DNA Composition of the Peri-Implant Sulcus Assessed By PCR and Sequencing Protocols6 Months
Microbial DNA Composition on the Dental Materials Assessed By PCR and Sequencing Protocols6 Months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026