Study on treatment for dentin hypersensitivity
Not Applicable
- Conditions
- dentin hypersensitivity
- Registration Number
- DRKS00004663
- Lead Sponsor
- Klinik für Zahnerhaltungskunde & Parodontologie, Universitätsklinikum Freiburg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
healthy patients with dentin hypersensitivity (18-70 years), informed consent
Exclusion Criteria
- ongoing dental or periodontal tratment or treatment of the oral mucosa
- insufficient oral hygiene
- allergy against an ingredient of the study tooth paste
- pregnancy or brast feeding
- heavy mental disorders
- intake of acidic drugs
- Vegetarian or vegan
- refulx disease
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method proof of reduction in dentin hypersensitivity by Schiff Test in 1, 4 and 8 weeks.
- Secondary Outcome Measures
Name Time Method proof of reduction in dentin hypersensitivity by Yeaple probe after 1, 4 and 8 weeks.