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Clinical Trials/NCT06397599
NCT06397599
Completed
Not Applicable

Denture Adhesive is a Patient Advantageous or Prosthetic Failure During Adaption Period: Randomized Control

Cairo University1 site in 1 country32 target enrollmentJanuary 12, 2023
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ConditionsDental

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dental
Sponsor
Cairo University
Enrollment
32
Locations
1
Primary Endpoint
patients satisfaction
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

Introduction: the complete denture wearers mainly complain of decrease of denture retention which affects on patient's quality of life Objective: to evaluate oral health-related quality of life (OHRQoL) of denture adhesive for completely edentulous denture wearers.

Material and methods : 32 patients(new denture wearers) were selected form prosthdontic clinic in three dental faculties in various region in Egypt, there were 22 females (68%) and 10 males (46%) were distributed in two groups: conventional group without adhesive and adhesive group with adhesive application n = 16;, in a cross over study. evaluation by Oral Health Impact Profile in Edentulous Adults (OHIP-EDENT) inventory at 1, 2 and 3 months after the insertion of new complete dentures. Data were analyzed using 2-way ANOVA test and Generalized Estimating Equations (GEEs), α = 0.05.

Detailed Description

32 patients(new denture wearers) were selected form prosthdontic clinic in three dental faculties in various region in Egypt, there were 22 females (68%) and 10 males (46%) were distributed in two groups: conventional group without adhesive and adhesive group with adhesive application n = 16;, in a cross over study. evaluation by Oral Health Impact Profile in Edentulous Adults (OHIP-EDENT) inventory at 1, 2 and 3 months after the insertion of new complete dentures. Data were analyzed using 2-way ANOVA test and Generalized Estimating Equations (GEEs), α = 0.05.

Registry
clinicaltrials.gov
Start Date
January 12, 2023
End Date
December 20, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sharaf Mohamed Yahia

lecturer

Cairo University

Eligibility Criteria

Inclusion Criteria

  • •completely edentulous

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

patients satisfaction

Time Frame: 6 months

questionnaires

Study Sites (1)

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