Skip to content

The effect of two different prophylaxis paste applying processes on color stability in office bleaching: 24 month clinical follow-up

The effect of two different prophylaxis paste applying processes on color stability in office bleaching: 24 month clinical follow-up

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220121003
Enrollment
300
Registered
2022-01-21
Start date
2018-02-18
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy person between the age group of 18 and 45 years. Healthy people

Interventions

Teeth were only bleaching without applying prophylaxis paste. ,After the application of Ultrapro (Ultradent, Cologne, Germany) prophylaxis paste, bleaching was done and after bleaching, prophylaxis pa
No Intervention Other,Experimental Other,Experimental Other,Experimental Other,Experimental Other
Control group,Ultrapro+Ultrapro prophylaxis paste,Cleanic+Cleanic prophylaxis paste,Ultrapro prophylaxis paste,Cleanic prophylaxis paste

Sponsors

Erciyes University Scientific Research Projects Foundation
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Between the ages of 18-45, Systemically healthy, Non-smoker, Suitable for oral hygiene whitening treatment, Periodontally healthy, Teeth have discoloration and are not aesthetically satisfied, No missing incisors, canines and premolars, The vital teeth of the teeth to be included in the study, The teeth to be included in the study do not have caries, abrasion, restoration and sensitivity, Patients who volunteered to participate in the study.

Exclusion criteria

Exclusion criteria: Systemic disease and drug use that prevent treatment, Smoking, Poor oral hygiene, Periodontal disease, Missing incisors, canines and premolars, Devitalization of the teeth to be included in the study, The presence of caries, abrasion, restoration and sensitivity in the teeth to be included in the study or the absence of a whitening indication, Patients' reluctance to participate in the study.

Design outcomes

Primary

MeasureTime frame
Spectrophotometer measurement 2 year CIE L* a* b* color system

Secondary

MeasureTime frame
Color difference calculation 2 year SPSS software program

Countries

Turkey

Contacts

Public ContactSemiha Ekrikaya

Erciyes University, Faculty of Dentistry

semihaekrikaya@gmail.com05072647366

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026