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

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified December 2011 by Mohammad Javad Shirani, Isfahan University of Medical Sciences.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01493232
First Posted: December 15, 2011
Last Update Posted: October 12, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Mohammad Javad Shirani, Isfahan University of Medical Sciences
December 12, 2011
December 15, 2011
October 12, 2017
October 2011
March 2012   (Final data collection date for primary outcome measure)
Patients' Satisfaction [ Time Frame: 1 year ]
method of measurement is Questionair
Same as current
Complete list of historical versions of study NCT01493232 on ClinicalTrials.gov Archive Site
Patients' Dissatisfaction [ Time Frame: 1 year ]
method of measurement Examination and Questionair
Same as current
Not Provided
Not Provided
 
Comparing Patient Satisfaction & Stress Distribution on Mandibular Ridge by Three Posterior Occlusal Scheme in Complete Denture
Comparing Patient Satisfaction & Stress Distribution on Mandibular Ridge by Three Posterior Occlusal Scheme in Complete Denture
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.
Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Triple (Participant, Care Provider, Outcomes Assessor)
Primary Purpose: Treatment
Edentulous
Other: buccalized occlusion
Making a set of complete denture with new Buccalized Occlusion that is different from current occlusion in my country. In this type just buccal casps of mandibular teeth will be connect to the central fossa of maxillary teeth and lingual casps have not contact.
Other Names:
  • K06.9
  • Disorder of gingiva and edentulous alveolar ridge, unspecified
  • Experimental: Denture, edentulous patient, treatment
    Dentures with different type of occlusion
    Intervention: Other: buccalized occlusion
  • Experimental: Denture, Edentulous patient, treatment
    Dentures with different type of occlusion
    Intervention: Other: buccalized occlusion
Shirani M, Mosharraf R, Shirany M. Comparisons of patient satisfaction levels with complete dentures of different occlusions: a randomized clinical trial. J Prosthodont. 2014 Jun;23(4):259-66. doi: 10.1111/jopr.12101. Epub 2013 Oct 19.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
15
May 2012
March 2012   (Final data collection date for primary outcome measure)

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
Sexes Eligible for Study: All
Child, Adult, Senior
Yes
Contact information is only displayed when the study is recruiting subjects
Iran, Islamic Republic of
 
 
NCT01493232
190052
IRCT201110097749N1 ( Other Grant/Funding Number: Medical Uuniversity of Isfehan 1244003 )
Yes
Not Provided
Not Provided
Mohammad Javad Shirani, Isfahan University of Medical Sciences
Isfahan University of Medical Sciences
Not Provided
Study Chair: Ramin Mosharraf, Prosthodontics Specialist Medical University of Isfahan
Isfahan University of Medical Sciences
December 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP