Patient Satisfaction and Clinical Experience of Dentists

September 30, 2021 updated by: Dr. Nadia Ereifej, University of Jordan

Association Between Patient Satisfaction With Complete Dentures and the Clinical Experience of the Treating Dentist

Rehabilitation of the edentulous patients has always been a challenge. The success of this treatment modality is not only affected by the patients' acceptance of his new dentures, but on his ability to use them which depends to a great extent on the quality of those dentures. It is strongly believed that the success of dental treatments is affected by the experience of a dentist. The aim of this study was to compare patient satisfaction with complete dentures provided by forth and fifth year dental students and prosthodontists at the University of Jordan Hospital one week and 8 weeks post insertion

Study Overview

Status

Completed

Detailed Description

After obtaining the ethical approval, questionnaires were distributed to a total of 60 patients who accepted to participate in this study. The 60 patients consisted of 2 groups. The first group included patients treated by fourth and fifth year students, the second group consisted of patients treated by prosthodontists with a minimum of 5 years of experience. The questionnaire was distributed to those patients 8 weeks post insertion of complete upper and lower dentures. The questionnaire was divided into 3 parts. the first part included demographic and contact information questions for the patient. The second part included examination to the upper and lower dental arches and a third part included questions that probed the patient's satisfaction with his upper and lower dentures in general. Furthermore, the questionnaire included questions about the patient's comfort with his dentures, whether he is satisfied with the esthetics, phonetics, retention, efficiency in mastication, and ease of cleaning. This part of the survey was adapted from the Oral Health Impact Profile (OHIP-EDENT) questionnaire.

Study Type

Observational

Enrollment (Actual)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Amman, Jordan, 11942
        • The university of Jordan

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The study population was completely edentulous patients attending the undergraduate students' clinic and specialty Prosthodontic clinics at the Jordan University Hospital in need of conventional complete dentures.

Description

Inclusion Criteria:The study population was completely edentulous patients attending the undergraduate students' clinic and specialty Prosthodontic clinics at the Jordan University Hospital in need of conventional complete dentures.

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Exclusion Criteria:

-

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Complete dentures fabricated by undergraduate students
Patient satisfaction was assessed regarding dentures fabricated by students and specialists after 8 weeks of delivery
Complete dentures fabricated by prosthodontists
Patient satisfaction was assessed regarding dentures fabricated by students and specialists after 8 weeks of delivery

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Patient satisfaction
Time Frame: 8 weeks after delivery
Visual Analogue Scale based questionnaire with 10 items regarding patient satisfaction
8 weeks after delivery
OHIP-EDENT
Time Frame: 8 weeks after delivery
20 item questionnaire regarding the oral health impact profile
8 weeks after delivery

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)

December 10, 2019

Primary Completion (Actual)

June 30, 2021

Study Completion (Actual)

July 31, 2021

Study Registration Dates

First Submitted

September 30, 2021

First Submitted That Met QC Criteria

September 30, 2021

First Posted (Actual)

October 13, 2021

Study Record Updates

Last Update Posted (Actual)

October 13, 2021

Last Update Submitted That Met QC Criteria

September 30, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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