Tooth Mousse and Fluoride in Dentin Hypersensitivity Treatment

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-01-31

Study Completion Date

2008-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

GC Tooth Mousse, a complex containing amorphous calcium phosphate (ACP) and casein phosphopeptide (CPP), is recommended in dentin hypersensitivity reduction due to its ability to block opened dentinal tubules. It acts synergistically with fluorine in slowing caries progression. Whether CPP-ACP can act synergistically with fluorine in the dentin hypersensitivity treatment is unknown. The aim of this study was to assess the effect of CPP-ACP combined with fluoride varnish in cervical dentin hypersensitivity treatment.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Efficacy of Formulated Eggshell Derived Nano-hydroxyapatite Containing Toothpaste With and Without Addition of Fluoride vs. Conventional Desensitizing Fluoride Containing Toothpaste in Management of Dentin Hypersensitivity

NCT06493500

Dentin Hypersensitivity Fluoride Nano-hydroxy Apatite

NOT_YET_RECRUITING PHASE1

Ca-hydroxyapatite, Fluoroapatite, and Mg-Zn-hydroxyapatite for Dentin Hypersensitivity Management

NCT04896294

Dentin Hypersensitivity

COMPLETED PHASE4

Three Different Topically Applied Materials as Non-invasive Treatment of Sensitivity in Permanent Teeth With Molar Incisor Hypomineralization

NCT07056855

Dentine Hypersensitivity

NOT_YET_RECRUITING NA

Effectiveness of Calcium Silicate and Sodium Fluoride Nanoparticles in The Management of Dentin Hypersensitivity

NCT06557980

Dentin Hypersensitivity

NOT_YET_RECRUITING NA

Effectiveness of Nanohydroxyapetite Paste on Reducing Dentin Hypersensitivity

NCT02936830

Dentin Hypersensitivity

COMPLETED PHASE4

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Dentin Hypersensitivity

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Tooth Mousse

No interventions assigned to this group

fluoride varnish

No interventions assigned to this group

Tooth Mousse + fluoride varnish

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* subjects with a minimum of three cervical hypersensitive teeth at both sides of the dental arch

Exclusion Criteria

* dentin hypersensitivity caused by caries lesions
* fracture of restoration
* chipped teeth
* marginal gaps
* post-operative sensitivity
* cracked-tooth syndrome, and which were confirmed by periapical radiographs and teeth with cervical fillings

Minimum Eligible Age

26 Years

Maximum Eligible Age

66 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No