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Conventional, Overdenture and Palateless Overdenture Oral Health Impact Comparison Study

NCT02731703 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 14

Last updated 2023-05-15

No results posted yet for this study

Summary

This study will identify and enroll patients already scheduled to receive guided maxillary implant placement with palateless overdenture. Standard clinical practice will be followed for this multi-stage process. The study purpose is to evaluate the degree of satisfaction during the standard progression in order to determine at which post edentulous stage patients achieve maximum satisfaction using the Oral Health Impact Profile 49 (OHIP 49).

Conditions

  • Jaw, Edentulous

Interventions

DEVICE

Overdenture treatment

Conventional, FDA-approved prosthetics will be used in accordance with their labeling and pre-study prescribed standard treatment approach

Sponsors & Collaborators

  • Dentsply Sirona Implants and Consumables

    collaborator INDUSTRY

  • University of North Carolina, Chapel Hill

    lead OTHER

Principal Investigators

  • Ingeborg De Kok, DDS MS · Associate Professor UNC School of Dentistry

Eligibility

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

Timeline & Regulatory

Start
2016-04-30
Primary Completion
2017-08-09
Completion
2023-01-04

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 NCT02731703 on ClinicalTrials.gov