- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05076968
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
Conditions
Intervention / Treatment
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
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-
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Amman, Jordan, 11942
- The university of Jordan
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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:
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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
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Patient satisfaction was assessed regarding dentures fabricated by students and specialists after 8 weeks of delivery
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Complete dentures fabricated by prosthodontists
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Patient satisfaction was assessed regarding dentures fabricated by students and specialists after 8 weeks of delivery
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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
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8 weeks after delivery
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OHIP-EDENT
Time Frame: 8 weeks after delivery
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20 item questionnaire regarding the oral health impact profile
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8 weeks after delivery
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
Other Study ID Numbers
- YOweis
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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