Hypersensitivity and Color Changes of Bleached Teeth Using Different Remineralizing Agents

NCT04875000 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 48

Last updated 2021-06-28

No results posted yet for this study

Summary

The aim of this in vivo study is to evaluate the post-bleaching enamel hypersensitivity and the possible color changes following the application of arginine and nano-hydroxyapatite remineralizing solutions after enamel bleaching using an in-office chemical bleaching agent. A commercial Fluoride remineralizing and desensitizing agent will be used as the control group. Following bleaching of the anterior teeth and then the application of the different tested remineralizing agents; the patients will be assessed for post-bleaching hypersensitivity using the visual analogue scale (VAS) to describe the severity of the hypersensitivity from mild to moderate to severe. On the other hand, the baseline shade and post-bleaching color changes will be evaluated using a shade guide. The data will be collected and tabulated then the statistical analysis will be performed.

The null hypothesis is that the different tested remineralizing agents will have a similar effect on the post-bleaching teeth hypersensitivity \& the color changes of the bleached teeth.

Conditions

  • Tooth Hypersensitivity

Interventions

OTHER

Remineralizing agent I application

Application of UltraEZ remineralizing agent to the bleached teeth

OTHER

Remineralizing agent II application

Application of 2.5% arginine solution to the bleached teeth

OTHER

Remineralizing agent III application

Application of 2.5% nano-hydroxyapatite solution to the bleached teeth

Sponsors & Collaborators

  • National Research Centre, Egypt

    lead OTHER

Principal Investigators

  • Lamiaa M Moharam, Ass. Prof · National Research Centre, Egypt

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-03-20
Primary Completion
2021-06-20
Completion
2021-06-20

Countries

  • Egypt

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Read the full study record

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View NCT04875000 on ClinicalTrials.gov