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PubMed2004

Comparison of effectiveness of two 10% carbamide peroxide tooth-bleaching systems using spectrophotometric measurements.

PURPOSE: The purpose of this study was to compare the color changes achieved with two commonly used bleaching systems on the basis of a spectrophotometric analysis. MATERIALS AND METHODS: Two commercially available 10% carbamide peroxide bleaching systems were used by a total of 48 individuals. Subjects who had intact natural maxillary anterior teeth void of any restorations or decay that had not been subjected to any prior bleaching were included. Opalescence 10% PF (Ultradent Products Inc., South Jordan, UT, USA) was used by 23 patients for 14 days, whereas Nite White Excel (Discus Dental, Culver City, CA, USA) was applied by 25 patients for the same duration. Tooth colors for the middle one-third region of maxillary central incisors and canines were measured with a spectrophotometer prior to bleaching and after 14 days of bleaching. Color difference deltaE and color coordinates L* (lightness), a* (redness), and b* (yellowness) of CIELAB color system (developed by the Commission Internationale de l'Eclairage) were calculated. RESULTS: Mean deltaE values for Opalescence ranged from 5.03 to 8.92 and from 5.84 to 9.61 for Nite White. The most significant factor of the color change was b* followed by L* and a*. L* values were higher after bleaching, whereas values for both a* and b* decreased. There were no significant differences between the two systems examined (p < .05).

Adult↗
PubMed2001

Enamel colour changes following whitening with 10 per cent carbamide peroxide: a comparison of orthodontically-bonded/debonded and untreated teeth.

The purpose of this study was to determine if a colour difference exists between teeth that had orthodontic appliances bonded to and debonded from them and untreated controls subjected to whitening with 10 per cent carbamide peroxide. The sample consisted of 20 pairs of first and second premolars extracted for orthodontic reasons. The contralateral surfaces were divided into an experimental and control group. The experimental group underwent orthodontic bonding/debonding procedures. Both groups were subjected to 4 hour whitening and 20 hour hydration sessions for 30 days. The L*a*b* colour system was chosen to evaluate any colour change and these changes were calculated by determining the delta E from the L*a*b* values using a colorimeter. Colour change readings were taken before and after each 4 hour whitening. Additional readings were taken at 48 hour intervals for 30 days following the cessation of active whitening. The results were analysed using statistical (ANOVA) and graphical analyses (alpha = 0.05). A colour change difference of 2 CIELAB units was set as being clinically significant. A mean clinical colour difference was found for enamel surfaces subjected to orthodontic bonding/debonding of attachments relative to control sites after whitening. Bonding and debonding procedures resulted in a significant colour difference between orthodontic bonded and control sites at the end of the active period, which became insignificant at the end of the 30 day period of monitoring. Both the control and debonded sites responded to whitening; however, the control sites responded initially to a greater extent; the orthodontic debonded sites did not respond until after 2 weeks of continuous whitening. After the 2 week period the improved response of the debonded sites decreased the colour difference between the two groups.

Algorithms↗
PubMed1996

Clinical efficacy of a degradable film-forming product containing carbamide peroxide to reduce tooth discolouration.

The methods used to lighten tooth discolouration while conserving the tooth structure have attracted much attention in a society which places a high value on esthetics. The purpose of this article is to present a home bleaching agent that uses a film-forming preparation containing carbamide peroxide (CP) which, while degrading, serves as a slow release delivery system of the bleaching agent. The efficacy of the preparation containing 3% CP and 10% CP on reduction of tooth discolouration is evaluated by a Chromameter in a double-blind placebo-controlled study. The effect of the tested bleaching agent on the gingival status, plaque accumulation and pulp sensitivity is also assessed.

Adolescent↗
PubMed2000

A clinical evaluation of carbamide peroxide and hydrogen peroxide whitening agents during daytime use.

BACKGROUND: Vital tooth bleaching for esthetic reasons has gained in popularity during the last few years. However, few studies have investigated the efficacy of daytime bleaching products. The purpose of this double-blind in vivo study was to evaluate the efficacy of 20 percent carbamide peroxide, or CP, and 7.5 percent hydrogen peroxide, or HP, during daytime use. The degree of color change, any color relapse, and tooth or gingival sensitivity were evaluated. METHODS: Twenty-four patients participated in this study. The bleaching gels were randomly applied to the right and left maxillary anterior teeth. Patients were shown how to place the two bleaching agents in a custom tray for one hour, twice a day for two weeks. Patients returned in one, two, three, six and 12 weeks for color evaluation with the colorimeter and shade guides as well as to have color slide photographs taken. The authors evaluated sensitivity by asking the patients to record daily for 21 days any tooth or gingival sensitivity they experienced. RESULTS: Use of the 20 percent CP resulted in significantly more lightness than the 7.5 percent HP during the first 14 days of the study, but at the end of the study, there was no significant difference between products with regard to tooth lightness. In addition, the authors found no statistically significant difference between products with regard to gingival or tooth sensitivity. CONCLUSIONS: Both CP and HP are effective at-home bleaching agents when daytime bleaching is preferred. CLINICAL IMPLICATIONS: Dentists who choose to use daytime bleaching can select either CP or HP.

Adult↗
PubMed1993

Efficacy of foam liner in 10% carbamide peroxide bleaching technique.

The purpose of this study was to determine if the use of a foam liner in a tray during the nightguard vital bleaching technique would cause a difference in the rate of bleaching or the final shade of the bleached teeth. Ten subjects were selected who had previously successfully bleached their maxillary arch by using a 10% carbamide peroxide solution. Vacuum-formed guards were fabricated for the mandibular arch so that one quadrant was covered with a conventional-style guard, and the other quadrant was covered with a foam-lined guard. All patients were successful in bleaching their mandibular arch. No patient reported any difference between the two quadrants in the rate of bleaching or in the final shade, nor was any difference apparent to the operators clinically or in photographic evaluation. It appears that the addition of a foam insert does not noticeably alter the clinical result of home bleaching. If bleaching is successful in one arch, it can be expected to be effective in the other arch.

Acrylic Resins↗
PubMedDate not supplied

A six-month study of two self-applied tooth whitening products containing carbamide peroxide.

Bleaching offers a non-interventive way of improving the appearance of sound, yet discolored anterior teeth. Until recently, the whitening agent was applied using a tray, but now other methods of delivering whitening agents, such as those using brush applicators, are available. This study investigated the tooth whitening efficacy of two novel, self-applied tooth whitening systems containing either 18% (Group 1) or 16.4% (Group 2) carbamide peroxide. Ninety-five subjects, ranging in age from 18 to 70 with anterior teeth A3 or darker, were recruited and randomly allocated to a group. The subjects were instructed to apply the formulation to all maxillary anterior teeth after brushing in the morning and evening. At baseline, two weeks and six months the upper six anterior teeth of the subjects were measured using the Vita shade guide tab system. In addition, the gingival health of the labial surfaces of the upper six anterior teeth was assessed using the Loee and Silness Gingival index (Loee & Silness, 1963) at baseline and at two weeks. The mean (SD) reduction in shade guide scores was 4.1 (2.4) shade guide tabs for subjects in Group 1, compared to 3.7 (2.6) shades for those in Group 2. This difference was not statistically significant (p=0.5). During the course of study, the gingivitis scores reduced from a mean (SD) of 0.91 (0.62) at baseline to 0.44 (0.55) at final examination (48% reduction). At the six-month recall, the mean (SD) reduction in shade guide scores was 2.3 (2.7) shade guide tabs for subjects in Group 1, compared to 2.5 (2.5) shades for those in Group 2. The different concentrations tested were found to be equally effective in improving the whiteness of upper anterior teeth by approximately four shades over a two-week period and the majority of the whitening benefit (c.60%) was sustained at six-month recall.

Adolescent↗
PubMed2003

The effect of a 10% carbamide peroxide home bleaching system on the gingival health.

Esthetics plays an important role in dentistry today. Because of an increased emphasis on beauty and health, cosmetic dentistry has been the thrust to the forefront of many practices. Many health products are used for bleaching teeth, but all side effects are not known. Tooth sensitivity and gingival irritation are the most common side effects, but they are typically mild and transient in nature. The aim of this investigation was to evaluate objectively the effect of 10% carbamide peroxide gel (Opalescence Utradent Inc, USA) on gingival health by measuring changes in Bleeding Index, Plaque Index, and Gingival Index. Eighteen subjects, 11 female and 7 male, age range 15-30 years (mean 24 years), were selected for the study as a convenient sample. Their teeth had either fluorosis, dental stains, smoking, or tetracycline staining. The Opalescence system was used as office monitored, at-home bleaching for three weeks. There was a statistically significant reduction in bleeding on probing (1% - 37%, p < or = 0.003), Plaque Index (4% - 50%, p < or = 0.000), and Gingival Index (2.5% - 34%, p < or = 0.002). Only two subjects reported tooth hypersensitivity, and none of the subjects complained about gingival irritation. There was a positive change in tooth color as far as staining was concerned. Further research including randomized controlled, double blind clinical trials is needed to confirm these findings and to examine other factors related to bleaching of teeth.

Adolescent↗
PubMedDate not supplied

Comparison of the clinical efficacy and safety of carbamide peroxide and hydrogen peroxide in at-home bleaching gels.

OBJECTIVE: The aim of this study was to evaluate the clinical efficacy of home-administered vital bleaching procedures and possible adverse effects derived from their use. One gel containing 3.5% hydrogen peroxide with a 5% potassium nitrate component (FKD, Kin Lab) was compared with a carbamide peroxide-based gel with a concentration of 10% (Opalescence, Ultradent). METHOD AND MATERIALS: Two sample groups were designed, each composed of 8 patients. All patients employed both bleaching products, 1 in the maxillary arch and the other in the mandibular arch on a random basis. The treatment was applied for 3 hours a day for 4 weeks. The degree of bleaching was evaluated using the Vita guide arranged by brightness. Dental sensitivity was measured with a specially designed 4-point scale. Gingival irritation was registered by the presence or absence of lesions in the marginal gingiva related to treatment. RESULTS: The degree of bleaching was similar with both products (4.8 Vita shade tabs). The hydrogen peroxide product with potassium nitrate provoked less dental sensitivity, although the difference between the 2 products was insignificant (P = .063). Gingival irritation appeared in 6 subjects, but was unrelated to the applied product. CONCLUSION: Under the conditions of this study, no statistically significant differences were detected between 3.5% hydrogen peroxide containing 5% potassium nitrate (FKD) and the 10% carbamide peroxide-based product (Opalescence).

Acrylic Resins↗
PubMed2004

Comparative tooth whitening efficacy of 18% carbamide peroxide liquid whitening gel using three different regimens.

OBJECTIVE: Recently, a novel paint-on liquid whitening gel--Colgate Simply White Clear Whitening Gel--which contains 18% carbamide peroxide, has been developed as a self-administered tooth bleaching system. The purpose of the present study was to determine the efficacy and safety of this product using alternate exaggerated or simplified treatment regimens. METHODOLOGY: This was a three-week clinical trial using a parallel, double-blind, stratified protocol with three different instructions for application: 1) twice-daily, no air-drying, and 15 minutes without eating/drinking; 2) three times daily, 30-second air-drying and 30 minutes without eating/drinking; or 3) four times daily, 30-second air-drying and 30 minutes without eating/drinking. One-hundred and twenty (120) healthy volunteers were balanced into three equal groups based on shade scores (A3 or darker). Clinical evaluations (shade guide, oral tissue health, gingival index and visual analog sensitivity score) were performed on each group at baseline and weekly for the next 21 days. At the conclusion of the study, a survey of the subjects' opinions on their assigned product regimen was also conducted. RESULTS: Subjects who used Colgate Simply White Clear Whitening Gel three and four times daily achieved the greatest shade improvement (5.88 +/- 1.53 shades, and 5.57 +/- 1.54, respectively). However, these values were only about one shade better than the value observed for the more convenient, twice-daily, "no-dry" regimen (4.51 +/- 1.77 shades), though they were statistically significant (p < 0.05). The result for the four-times daily protocol was not statistically different from the three-times group. Also, no differences were observed between the groups concerning oral tissue health, gingival index or tooth sensitivity, and no adverse effects were observed or reported regardless of the regimen used. Surveys completed by the subjects showed that those who used the twice-daily, "no-dry" regimen found the product to be the easiest to use, the most comfortable and the most pleasant tasting. CONCLUSION: It can be concluded from the clinical data that three or four applications of Colgate Simply White Clear Whitening Gel per day provided better efficacy. In addition, the use of the whitening gel twice daily, even without "dry time" and only 15 minutes without eating/drinking, yielded results that were comparable to previously reported results using the original on-label directions. The potential additional benefit to the "simplified regimen" is that it was perceived to be the most convenient and comfortable. The use of Colgate Simply White Clear Whitening Gel up to four times daily for up to three weeks is also safe, and the tendency of abusing the product with more frequent daily use may be deterred by the inconvenience reported by the study subjects.

Adult↗