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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: ClinicalTrials.gov
Last refreshed on: 6 October 2015
Main ID:  NCT02203279
Date of registration: 28/07/2014
Prospective Registration: No
Primary sponsor: Damascus University
Public title: Evaluation of Three Hard Relining Materials in Complete Dentures
Scientific title: Evaluation of Three Hard Relining Materials in Complete Dentures: An In-vivo Study
Date of first enrolment: July 2014
Target sample size: 36
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT02203279
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment  
Phase:  N/A
Countries of recruitment
Syrian Arab Republic
Contacts
Name:     Muhannad Alssadi, DDS MSc PhD
Address: 
Telephone:
Email:
Affiliation:  Associate Professor, Removable Prosthodontics Department, University of Damascus Dental School, Damascus
Name:     Omar Teriaky, DDS MSc
Address: 
Telephone:
Email:
Affiliation:  PhD student, Department of Removable Prosthodontics, University of Damascus Dental School, Damascus
Key inclusion & exclusion criteria

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
Health Condition(s) or Problem(s) studied
Complete Mandibular Dentures With Poor Retention
Intervention(s)
Other: Flexacryl
Other: Rebase II Fast
Other: Vertex
Primary Outcome(s)
Supporting Alveolar Mucosa Status_3 [Time Frame: This will be measured at three months following relining]
Color Stability_3 [Time Frame: This will be assessed at three moths following relining]
Supporting Alveolar Mucosa Status_6 [Time Frame: This variable will be assessed at six months following relining]
Secondary Outcome(s)
Peeling_3 [Time Frame: This variable is going to be assessed at three months following relining]
Color Stability_6 [Time Frame: This be assessed at six months following relining]
Satisfaction_3 [Time Frame: This is going to be measured at three months following relining]
Satisfaction_6 [Time Frame: This is going to be measured at six months following relining]
Peeling_6 [Time Frame: This variable is going to be assessed at six months following relining]
Secondary ID(s)
UDDS-RemPro-02-2014
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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