- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06074952
Comparing the Color Stability of Acrylic Denture Teeth in Different Staining Solutions
Comparing the Color Stability of Acrylic Denture Teeth in Different Staining Solutions-In Vitro Experimental Trial
The purpose of this (In Vitro Experimental Trial) is to assess (the color stability of acrylic denture teeth) in( different staining solutions) at (time intervals).
The (acrylic denture) teeth will be immersed in (staining solutions) and the values will be recorded at (different time intervals).
Three groups will be made:
- Group A- Control group
- Group B- Study group
- Group C- Study group
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In this study, two brands of acrylic denture teeth will be used for comparing the color stability in different staining solutions at time intervals. Identified staining substances which are tea, coke, and turmeric will be used for the staining effect evaluation. Honey solution will be used for the first time as a staining agent because honey consumption is most common in all the age groups due to its therapeutic effects. In this study, all the color values will be measured by using Portable Colorimeter (NH300, China).These values will be measured before the immersion and then after 7-days, 15-days and 21-days interval after the immersion in the solutions.
The purpose of this study is to assess the color stability of acrylic denture teeth in different staining solutions at time intervals.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Huda Adil, BDS, FCPS-II Resident
- Phone Number: 03112089558
- Email: hudaadildaffodils@gmail.com
Study Locations
-
-
Sindh
-
Karachi, Sindh, Pakistan
- Recruiting
- Altamash Institute of Dental medicine and Karachi University
-
Contact:
- Huda Adil, BDS, FCPS-II Resident
- Phone Number: 03112089558
- Email: hudaadildaffodils@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Maxillary central incisor teeth
- Teeth with normal flat labial surfaces
- Inter-penetrating polymer network (IPN) teeth
Exclusion Criteria:
- Posterior teeth
- Teeth with stains
- Fractured and worn-out teeth
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Group A- Control group
Control group will use distilled water as a control medium
|
Distilled water will be used as a control medium in the control group.
In group B, tea, coke, turmeric, and honey solutions will be used.
In group C, tea, coke, turmeric, and honey solutions will be used.
|
Other: Group B- Study group
In this group, 4 sub-groups will be made in which acrylic teeth of Welbite brand will be immersed in tea, coke, turmeric, and honey solutions.
|
Distilled water will be used as a control medium in the control group.
In group B, tea, coke, turmeric, and honey solutions will be used.
In group C, tea, coke, turmeric, and honey solutions will be used.
|
Other: Group C- Study group
In this group, 4 sub-groups will be made in which acrylic teeth of the Huge Kaili brand will be immersed in tea, coke, turmeric, and honey solutions.
|
Distilled water will be used as a control medium in the control group.
In group B, tea, coke, turmeric, and honey solutions will be used.
In group C, tea, coke, turmeric, and honey solutions will be used.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Color stability
Time Frame: The acrylic teeth will be measured at 7-days, 15-days, and lastly at 21-days interval.
|
Color stability of acrylic denture teeth in different staining solutions will be measured by using colorimeter at different time intervals.
|
The acrylic teeth will be measured at 7-days, 15-days, and lastly at 21-days interval.
|
Collaborators and Investigators
Investigators
- Study Director: Naseer Ahmed, BDS,FCPS, Altamash Institute of dental medicine
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- AltamashHC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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