Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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6 October 2015 |
Main ID: |
NCT02203279 |
Date of registration:
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28/07/2014 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Evaluation of Three Hard Relining Materials in Complete Dentures
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Scientific title:
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Evaluation of Three Hard Relining Materials in Complete Dentures: An In-vivo Study |
Date of first enrolment:
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July 2014 |
Target sample size:
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36 |
Recruitment status: |
Completed |
URL:
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https://clinicaltrials.gov/show/NCT02203279 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Syrian Arab Republic
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Contacts
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Name:
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Muhannad Alssadi, DDS MSc PhD |
Address:
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Telephone:
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Email:
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Affiliation:
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Associate Professor, Removable Prosthodontics Department, University of Damascus Dental School, Damascus |
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Name:
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Omar Teriaky, DDS MSc |
Address:
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Telephone:
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Email:
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Affiliation:
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PhD student, Department of Removable Prosthodontics, University of Damascus Dental School, Damascus |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Age between 45-80 year,
- complete maxillary and lower dentures
- Mandibular dentures with poor retention
Exclusion Criteria:
- Patients with good stability of mandibular dentures.
- Partial maxillary edentulous patients
Age minimum:
47 Years
Age maximum:
78 Years
Gender:
Male
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Health Condition(s) or Problem(s) studied
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Complete Mandibular Dentures With Poor Retention
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Intervention(s)
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Other: Flexacryl
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Other: Rebase II Fast
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Other: Vertex
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Primary Outcome(s)
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Supporting Alveolar Mucosa Status_3
[Time Frame: This will be measured at three months following relining]
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Color Stability_3
[Time Frame: This will be assessed at three moths following relining]
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Supporting Alveolar Mucosa Status_6
[Time Frame: This variable will be assessed at six months following relining]
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Secondary Outcome(s)
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Peeling_3
[Time Frame: This variable is going to be assessed at three months following relining]
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Color Stability_6
[Time Frame: This be assessed at six months following relining]
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Satisfaction_3
[Time Frame: This is going to be measured at three months following relining]
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Satisfaction_6
[Time Frame: This is going to be measured at six months following relining]
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Peeling_6
[Time Frame: This variable is going to be assessed at six months following relining]
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Secondary ID(s)
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UDDS-RemPro-02-2014
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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