Comparative evaluation of the effects of laser Diode 980 nm and CPP-ACP paste on treatment of dentinal hypersensitivity
Not Applicable
Recruiting
- Conditions
- Dental Hypersensitivity.Disorder of teeth and supporting structures, unspecifiedK08.9
- Registration Number
- IRCT20150613022699N5
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Inclusion Criteria:Patients reffering to dental faculty of isfahan university of medical sciences who have cervical dentin hypersensitivity in at least three teeth in three separate half jaw
Patients will be available for three months during the study and sign the form of consent form .
Teeth do not need restoration treatment
Exclusion Criteria
Erosion,attrition,dental cracks,pulpitis,periodontal disease
Active caries,restorated teeth,Crown fracture
Patients who have taken anti-histamine ,anti-depression and analgesics one month before the study
Pregnant and lactating women
Smokers
Patients who have received anti-Sensitivities toothpaste over the past 6 weeks.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Initial improvement of dental hypersensitivity. Timepoint: A dental sensitivity is measured in a month before and after therapeutic intervention every week. Method of measurement: According to the visual analogue scale.
- Secondary Outcome Measures
Name Time Method ong-term improvement in dental hypersensitivity. Timepoint: One week,30 days and 60 days after the last therapeutic intervention. Method of measurement: According to the visual analogue scale.