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Clinical study of the bleaching tooth paste with various concentration of bleaching agent

A Randomized controlled clinical trial to assess the clinical efficacy of bleaching tooth paste with various concentration of hydrogen peroxide (HP)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002877
Enrollment
120
Registered
2018-05-18
Start date
2018-05-15
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Others(Non pharmaceutical products) : There is no difference of application method between groups. The four experimental groups were divided according to the concentration of bleaching agent of toothp
group1, 0.75&#37
of HP containing toothpaste (Toothwhold white)
group2, 0.75&#37
of HP containing toothpaste (Vussen7)
group3, 1.5&#37
of HP containing toothpsate(Its white)
group4,2.8&#37
of HP containing toothpaste (Vussen28). The volunteers brush their tooth using the experimental materials manually for 12weeks, and the toothbrushing is instructed for three times per day.

Sponsors

Kyung Hee University Dental Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria is as follow: 1)Patients who have the discolored teeth between the ages of 18 and 50 volunteered for this study. 2) ASA physical classification, class 1 or 2 3) voluteers who thoroughly understand and agree to this clinical trial 4) Prior to involve this clinical trial, the shade of the maxillary incisor was evaluated by the spectrophotometer, and the patients who presented the shade above A2 was included.

Exclusion criteria

Exclusion criteria: Exclusion criteria was as follow; 1)the patients who have the history of allergy to the bleaching agent; 2)who have the extensive prosthesis or restorations in the incisors; 3)who have the orthodontic brackets; 4)who have the tooth with endodontic treatment, 5)who have the intrinsic discoloration due to the tetracycline or fluorosis, 6)who have gingival recession, exposure of the dental root or periodontal disease; 7)who are pregnant ; 8)who has the personal relationship to the researchers, 9)who are judged as improper to participate this clinical trial, etc.

Design outcomes

Primary

MeasureTime frame
Shade improvement

Secondary

MeasureTime frame
Teeth hypersensitivity

Countries

Korea, Republic of

Contacts

Public ContactJi-Hyun Jang

Kyung Hee University Dental Hospital

zangzi1021@hanmail.net+82-2-958-9330

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026