Tooth Mousse and Fluoride in Dentin Hypersensitivity Treatment
This study has been completed.
Sponsor:
Huazhong University of Science and Technology
Collaborator:
National Natural Science Foundation of China
Information provided by:
Huazhong University of Science and Technology
ClinicalTrials.gov Identifier:
NCT00926484
First received: June 22, 2009
Last updated: NA
Last verified: June 2009
History: No changes posted
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Purpose
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.
| Condition |
|---|
|
Dentin Hypersensitivity |
| Study Type: | Observational |
| Study Design: | Observational Model: Case-Only Time Perspective: Retrospective |
| Official Title: | Combined Tooth Mousse and Fluoride Varnish in Dentin Hypersensitivity Treatment |
Resource links provided by NLM:
Further study details as provided by Huazhong University of Science and Technology:
Primary Outcome Measures:
- ANOVA [ Time Frame: June 2008 ] [ Designated as safety issue: Yes ]
Secondary Outcome Measures:
- T-test [ Time Frame: June 2008 ] [ Designated as safety issue: Yes ]
| Enrollment: | 30 |
| Study Start Date: | January 2007 |
| Study Completion Date: | June 2008 |
| Primary Completion Date: | January 2008 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
| Tooth Mousse |
| fluoride varnish |
| Tooth Mousse + fluoride varnish |
Eligibility| Ages Eligible for Study: | 26 Years to 66 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Study Population
primary care clinic
Criteria
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
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00926484
Locations
| China, Hubei | |
| Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology | |
| Wuhan, Hubei, China, 430030 | |
Sponsors and Collaborators
Huazhong University of Science and Technology
National Natural Science Foundation of China
Investigators
| Study Chair: | Xuejin Tao, Doctor | Huazhong University of Science and Technology |
More Information
Additional Information:
Publications:
| Responsible Party: | Weimin Chen, Tongji Hospital, Huazhong University of Science and Technology |
| ClinicalTrials.gov Identifier: | NCT00926484 History of Changes |
| Other Study ID Numbers: | TF87330244 |
| Study First Received: | June 22, 2009 |
| Last Updated: | June 22, 2009 |
| Health Authority: | China: National Natural Science Foundation |
Keywords provided by Huazhong University of Science and Technology:
|
Dentin hypersensitivity Tooth Mousse fluoride varnish |
Additional relevant MeSH terms:
|
Dentin Sensitivity Hypersensitivity Tooth Diseases Stomatognathic Diseases Immune System Diseases Fluorides, Topical |
Fluorides Cariostatic Agents Protective Agents Physiological Effects of Drugs Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 16, 2013