Evaluation and comparison of the effects of bleaching gel containing 1% sodium hexametaphosphate on color stability and dental sensitivity during and after bleaching: a randomized, triangular blinded clinical trial study.
Phase 2
- Conditions
- Bad teeth color.
- Registration Number
- IRCT20180630040294N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Patients need to be treated for bleaching for which they are given this treatment so that the teeth that are needed to bleach for them are free of decay or repairs.
Patients in favorable general and oral health conditions.
Patients without dental sensitivity by touch and thermal stimuli.
Exclusion Criteria
Patients with a history of disease or long-term use of the drug.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Tooth color by spectrophotometer and tooth sensitivity by VAS system. Timepoint: Before and after treatment, immediately after treatment and 24 hours after treatment, one week after treatment, one month after treatment and 3 months after treatment. Method of measurement: Tooth color by spectrophotometer and tooth sensitivity by VAS system.
- Secondary Outcome Measures
Name Time Method