Dentin Sensitivity Clinical Trial
Official title:
Long-term Clinical Evaluation of In-office Dental Bleaching Using a Violet Light (405-410 nm)
NCT number | NCT03207204 |
Other study ID # | 010 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | July 2, 2017 |
Est. completion date | July 2, 2020 |
Verified date | November 2020 |
Source | University of Sao Paulo |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective of this clinical study is to evaluate the effect of the whitening treatment performed with the violet LED light (405-410 nm), with or without a bleaching gel, on the tooth color changes (immediate and long-term), tooth sensitivity, satisfaction of participants in relation to the technique and impact on their quality of life. After being informed of the objectives of the study, 200 participants will be selected and randomly divided into a treatment group (n = 25): G1 - 35% hydrogen peroxide (HP) (4 sessions, 1 session/week); G2 - 30% carbamide peroxide (CP) (4 sessions, 1 session/week); G3 - Violet LED (405-410 nm, 4 sessions, 1 session/week); G4 - Violet LED (405-410 nm, 4 sessions, 2 sessions/week); G5 - Violet LED associated to 35% hydrogen peroxide (4 sessions, 1 session / week); G6 - Violet LED associated to 30% carbamide peroxide (4 sessions, 1 session / week); G7 - hybrid technique HP (Violet LED + application of 35% hydrogen peroxide + violet LED) (4 sessions, 1 session/week); G8 - Hybrid technique CP HP (Violet LED + application of 30% carbamide peroxide + violet LED) (4 sessions, 1 session/week). The color evaluation will be performed at predetermined times (before and immediately after treatment, 14 days after completion of bleaching and 3, 6 and 12 months after completion of bleaching), and quantitatively evaluated by colorimetric tests (objective and subjective) and spectrophotometry. In addition, it will be evaluated the tooth sensitivity during and after (48 hours) tooth whitening (VAS Scale), satisfaction with the treatment and impact on quality of life (OHIP-14 questionnaire). The data, except for survey data of satisfaction (descriptive evaluation), will be subjected to statistical analysis to determine the homogeneity and normality of the sample and for comparison between treatment groups, considering a 5% significance level.
Status | Completed |
Enrollment | 200 |
Est. completion date | July 2, 2020 |
Est. primary completion date | December 2, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 30 Years |
Eligibility | Inclusion Criteria: - Presence of all the teeth, without restorations or caries on anterior teeth. - Patients presenting the canine tooth color A3 (according to Vita classical scale) or darker. Exclusion Criteria: - Patients presenting systemic pathologies - Patients presenting periodontal diseases - Smokers or patients with systematic use of alcohol - Patients presenting teeth with color alterations by tetracycline, fluorosis, endodontic treatments. - Patients with historic of self-referenced sensitivity - Pregnant or Breastfeeding period patients - Presence of restorations on anterior teeth - Patients presenting bruxism or systematic use of analgesics or anti-inflammatory drugs |
Country | Name | City | State |
---|---|---|---|
Brazil | School of Dentistry of USP | São Paulo | SP |
Lead Sponsor | Collaborator |
---|---|
University of Sao Paulo |
Brazil,
Bernardon JK, Sartori N, Ballarin A, Perdigão J, Lopes GC, Baratieri LN. Clinical performance of vital bleaching techniques. Oper Dent. 2010 Jan-Feb;35(1):3-10. doi: 10.2341/09-008CR. — View Citation
Boushell LW, Ritter AV, Garland GE, Tiwana KK, Smith LR, Broome A, Leonard RH. Nightguard vital bleaching: side effects and patient satisfaction 10 to 17 years post-treatment. J Esthet Restor Dent. 2012 Jun;24(3):211-9. doi: 10.1111/j.1708-8240.2011.00479.x. Epub 2011 Oct 11. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Color alteration | The color measurement will be blind, in predetermined time (12 months after the treatment). It will be performed with a clinical spectrophotometer. | 12 months after the treatment | |
Secondary | Dental sensitivity | The evaluation of dental sensitivity will be measured with a Visual analogue scale (VAS). It will be performed immediately after the treatment and 48 hours after the treatment. | Immediately after the treatment and 48 hours after the treatment | |
Secondary | Patient satisfaction regarding the treatment | The patient satisfaction regarding the treatment will be measured with a questionnaire for self-evaluation of the treatment, and will be applied 14 days after the end of treatment, 3 months after, 6 months after and 12 months after. | 14 days after the end of treatment, 3 months after, 6 months after and 12 months after | |
Secondary | Quality of life of the patients | The evaluation of quality of life of the patients will be performed with the OHIP-14 questionnaire, which will be applied after the end of the treatment. | Immediately after the end of bleaching | |
Secondary | Color change throughout 12 months with a visual color scale | The evaluation will be performed with a visual color scale | Before, immediately after, 14 days, 3 months, 6 months and 12 months after bleaching | |
Secondary | Color change throughout 6 months with a clinical spectrophotometer | The evaluation will be performed with a clinical spectrophotometer | Before, immediately after, 14 days, 3 months and 6 months after bleaching |
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