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Abutment Macro Design and Peri-implant Tissues

NCT02546713 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2022-04-13

No results posted yet for this study

Summary

The aim of this study is to evaluate the effect of abutment macro-design on soft and hard tissue responses. This trial is designed as a randomized controlled clinical study in which two groups of fourteen partially edentulous patients will have as part of their treatment one implant placed in the maxillary premolar region.

Conditions

  • Edentulous

Interventions

OTHER

Abutment with concave subcritical contour

Implants will be restored with abutments with concave configuration of the subcritical contour

OTHER

Abutment with convex subcritical contour

Implants will be restored with abutments with convex configuration of the subcritical contour

Sponsors & Collaborators

  • Dentsply Sirona Implants and Consumables

    collaborator INDUSTRY

  • Nova Southeastern University

    lead OTHER

Principal Investigators

  • Theofilos Koutouzis, DDS · Nova Southeastern University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-12-31
Primary Completion
2020-12-31
Completion
2021-11-30

Countries

  • United States

Study Locations

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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 NCT02546713 on ClinicalTrials.gov