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NCT03184883 Clinical Trial

Comparative Study Between Acrylic and Flexible Dentures

Health Knowledge, Attitudes, Practice Clinical Trial

Official title:
Comparative Study of Conventional Versus Flexible Mandibular Single Complete Denture

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT03184883
Other study ID # evidence committee
Secondary ID
Status Not yet recruiting
Phase N/A
First received June 2, 2017
Last updated July 19, 2017
Start date September 1, 2017
Est. completion date December 1, 2017

Study information
Verified date June 2017
Source Cairo University
Contact Marianne Azer, Bachelor
Phone 01227243531
Email marianne.fouad@dentistry.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

comparing the effect of conventional mandibular single denture with flexible mandibular single denture on tissue and patient's satisfaction

Description:

comparing the effect of conventional mandibular single denture with flexible mandibular single denture on tissue by keratinization index through PAP stain and patient's satisfaction through a questionnaire

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 17
Est. completion date December 1, 2017
Est. primary completion date October 1, 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

1. Mandibular flat ridge

2. Patient with opposing natural teeth or satisfactory fixed prostheses

3. Angle class I Maxillimandibular relationship

4. No intraoral soft and hard tissue pathosis

5. Non smokers

6. Patients with no previous denture experience

7. Patients having last extraction at least 6 month before denture construction

Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

  • Health Knowledge, Attitudes, Practice

Intervention

Procedure:
• single conventional denture
mandibular conventional denture with soft liner
• single flexible denture
mandibular flexible compete denture

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Outcome
Type Measure Description Time frame Safety issue
Primary Cytological changes manifested as keratinization index Objective Outcome: measuring the cytological changes manifested as keratinization index 6 months
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