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Clinical Trials/NCT01493232
NCT01493232UnknownNot Applicable

Comparing Patient Satisfaction & Stress Distribution on Mandibular Ridge by Three Posterior Occlusal Scheme in Complete Denture

Isfahan University of Medical Sciences2 sites in 2 countries15 target enrollmentStarted: October 2011Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
15
Locations
2
Primary Endpoint
Patients' Satisfaction

Study Overview

Brief Summary

In this randomized clinical trial to compare the patients' satisfaction of complete dentures with different occlusal forms, after simple randomized sampling of 15 participant that will be signed informed consent and their latest teeth was extracted 3 month ago, will be selected. For each participant, it will be made 3 set of complete dentures that are variable in occlusion only. During the study, dissatisfied participants can leave it. Each set will be inserted for 1month in 5 participant randomly. The participants will be examined in two stages, after a day and after a week. At the end of month the questionaire will be filled out and the pressure under the mandibular denture base will be measured with the pressure sensors. Then the second and third denture will be inserted simultaneously.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Outcomes Assessor)

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • edentulous patients
  • at least 3 month ago the latest teeth was extracted
  • ideal jaw relation
  • signing the informed consent

Exclusion Criteria

  • uncontrolled systemic disease
  • mentally problem
  • dissatisfaction for keeping on the study

Arms & Interventions

Denture, edentulous patient, treatment

Experimental

Dentures with different type of occlusion

Intervention: buccalized occlusion (Other)

Denture, Edentulous patient, treatment

Experimental

Dentures with different type of occlusion

Intervention: buccalized occlusion (Other)

Outcomes

Primary Outcomes

Patients' Satisfaction

Time Frame: 1 year

method of measurement is Questionair

Secondary Outcomes

  • Patients' Dissatisfaction(1 year)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mohammad Javad Shirani

Mohammad Javad Shirani, Isfahan University of Medical Sciences, Faculty of dentistry,Dnt.mui.ac.ir, Perincipal investigator, Dental student.

Isfahan University of Medical Sciences

Study Sites (2)

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