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NCT00926484 Clinical Trial

Tooth Mousse and Fluoride in Dentin Hypersensitivity Treatment

Dentin Hypersensitivity Clinical Trial

Official title:
Combined Tooth Mousse and Fluoride Varnish in Dentin Hypersensitivity Treatment

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00926484
Other study ID # TF87330244
Secondary ID
Status Completed
Phase N/A
First received June 22, 2009
Last updated June 22, 2009
Start date January 2007
Est. completion date June 2008

Study information
Verified date June 2009
Source Huazhong University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date June 2008
Est. primary completion date January 2008
Accepts healthy volunteers No
Gender All
Age group 26 Years to 66 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
China Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan Hubei

Sponsors (2)
Lead Sponsor Collaborator
Huazhong University of Science and Technology National Natural Science Foundation of China

Country where clinical trial is conducted

China, 

References & Publications (1)

Kowalczyk A, Botulinski B, Jaworska M, Kierklo A, Pawinska M, Dabrowska E. Evaluation of the product based on Recaldent technology in the treatment of dentin hypersensitivity. Adv Med Sci. 2006;51 Suppl 1:40-2. — View Citation

Outcome
Type Measure Description Time frame Safety issue
Primary ANOVA June 2008
Secondary T-test June 2008
See also
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Completed NCT04225247 - Efficacy of Seventh Generation Bonding Agents as Short-Term Desensitizers Among Patients With Hypersensitivity Phase 3
Completed NCT04887181 - The Effects of Different Dentin Hypersensitivity Treatment Methods on Quality of Life N/A
Not yet recruiting NCT03061383 - Reduction of Dentine Hypersensitivity Using 8% Arginine Based Toothpaste and 8% Strontium Acetate Based Toothpaste (DH) N/A
Recruiting NCT03076944 - Evaluation of Desensitization Protocols in Reduction of Dentin Hypersensitivity N/A
Recruiting NCT06264453 - A Study to Evaluate the Efficacy and Safety of KH001 in Patients With Dentin Hypersensitivity Phase 2
Recruiting NCT03083496 - Clinical Evaluation of Different Potassium Oxalate Concentrations in Dentin Hypersensitivity Treatment N/A
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