Esthetic Expectations of Edentulous Patients Followed in a French Dental Clinic

September 12, 2017 updated by: Dr Braud Adeline, Hôpital Rothschild

Esthetic is a major factor in complete denture (CD) success. Patient involvement in esthetic project plays a crucial role in denture acceptance and patient satisfaction. Historically, teeth choice and arrangement were made according to Frush and Ficher's recommendations focusing on natural looking of esthetics. Dentists may also propose to restore the dentate state looking for denture when preextraction data are available. Recently, a patient-centered approach based on attractivity has been proposed and may lead to in an appearance transcending the laws of nature.

The aim of the present study was to investigate actual denture esthetic expectations in a French edentate population followed in a university dental clinic (Rothschild Hospital , AP-HP).

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Inclusion criteria : being currently edentulous within at least within the maxillary arch, literate French speakers, willing and able to complete the survey in a single sitting. Clinical data collection was made by a unique examiner and concerned length of edentulism, antagonist arch, existence of preextraction data, smile attractivity opinion. The respondents completed a questionnaire identifying their age, sex, educational and income level. Patients were also asked for their denture look preference among 4 esthetic projects: 1) restoring pre-extraction (dentate) looking, 2) restoring actual denture looking, 3) creating natural looking, 4) creating perfect looking, 5) no opinion. Each project was explained similarly by the same examiner. Statistical analysis using a Pearson Chi-squared test at a 0.05 level of significance was conducted for associations between esthetic projects preference and tested variables.

Study Type

Observational

Enrollment (Actual)

42

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Totally edentulous subjects (20 women, 22 men, mena aged: 67.9 ± 12.2 years) attending maxillary CD in the department of prosthodontics of the Hopital Rothschild (AP-HP) are concerned by recruitment and are proposed to participate.

Description

Inclusion criteria : Currently edentulous maxillary arch, literate French speakers, willing and able to complete the survey in a single sitting. Inclusion Criteria:

Exclusion Criteria: Aged under 18 years.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
esthetic preferred project
Time Frame: Esthetic expectation evaluated at date of inclusion
Patients were asked for their denture-looking expectations among 4 esthetic projects: 1) restoring pre-extraction dentate looking, 2) restoring actual denture looking, 3) creating natural looking, 4) creating perfect looking, 5) no opinion.
Esthetic expectation evaluated at date of inclusion

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
age
Time Frame: evaluated at date of inclusion
Respondents completed a questionnaire identifying their age (in years)
evaluated at date of inclusion
gender
Time Frame: evaluated at date of inclusion
Respondents completed a questionnaire identifying their gender (man or woman)
evaluated at date of inclusion
educational level
Time Frame: evaluated at date of inclusion
Respondents completed a questionnaire identifying their educational level : last degree (no degree at al, French General Certificate Secondary Education, High School Diploma, Vocational Training Certificate taken at Secondary School, university degree)
evaluated at date of inclusion
month income level,
Time Frame: evaluated at date of inclusion
Respondents completed a questionnaire identifying their income level each month : in euros
evaluated at date of inclusion
length of edentulism,
Time Frame: evaluated at date of inclusion
Respondents completed a questionnaire identifying the duration of edentulism (in years)
evaluated at date of inclusion
smile attractivity opinion
Time Frame: evaluated at date of inclusion
Respondents completed a questionnaire identifying their smile attractivity opinion Respondents completed a questionnaire identifying the most attractive smile among 4 esthetic situations : preextraction-looking smile, denture-like smile, natural-like smile, perfect smile.
evaluated at date of inclusion
preextraction data available
Time Frame: evaluated at date of inclusion
Respondents completed a questionnaire identifying the existence of preextraction data available (available or not available)
evaluated at date of inclusion

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2016

Primary Completion (Actual)

September 1, 2017

Study Completion (Actual)

September 1, 2017

Study Registration Dates

First Submitted

September 9, 2017

First Submitted That Met QC Criteria

September 12, 2017

First Posted (Actual)

September 14, 2017

Study Record Updates

Last Update Posted (Actual)

September 14, 2017

Last Update Submitted That Met QC Criteria

September 12, 2017

Last Verified

September 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • 01 (Miami VAHS)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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