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Maxillary 3-implant Removable Prostheses Without Palatal Coverage on Locator Abutments

NCT02957487 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 32

Last updated 2019-05-16

No results posted yet for this study

Summary

The aims of this clinical study conducted at a dental specialty clinic in Drammen, Norway are to assess the clinical outcomes of patients with an edentate upper jaw having been treated with a removable full prosthesis supported by 3 implants to restore function and aesthetics. Clinical variables beyond implant dimensions and intraoral location, such as recall routines, maintenance needs, patient satisfaction and quality of life, will also be appraised and contrasted with an aim to elucidate their association with clinical outcomes. Specific evaluation will be done with regard to the following outcome criteria:

* crestal bone levels and periodontal conditions around implants
* incidence rates of biological, technical, traumatic failures / complications related to implants
* incidence rates of biological, technical, mechanical, esthetic failures/complications with prosthesis and prosthetic components A secondary objective is to identify the different risk factors for biological failures / complications, including the influence of medical conditions and tobacco use.

Conditions

  • Edentulous Maxilla

Interventions

DEVICE

Denture supported by 3 dental implants

Metal-reinforced denture without palatal coverage incorporating nylon rings retained by friction to Locator abutments fitted on top of dental implants

Sponsors & Collaborators

  • University of Tromso

    lead OTHER

Principal Investigators

  • Asbjørn Jokstad, DDS, PhD · UiT The Arctic University of Norway

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2018-09-28
Completion
2018-09-28

Countries

  • Norway

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 NCT02957487 on ClinicalTrials.gov