Skip to content

Study on the Whitening and Sensitive Relief Effects of LESENING Teeth Strips Containing 3% Hydrogen Peroxide and 1.5% Potassium Nitrate

Study on the Whitening and Sensitive Relief Effects of LESENING Teeth Strips Containing 3% Hydrogen Peroxide and 1.5% Potassium Nitrate

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100861
Enrollment
Unknown
Registered
2025-04-16
Start date
2024-06-08
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Tooth extrinsic discoloration and tooth hypersensitivity

Interventions

Experimental group:Participants in the experimental group were given LESEING strips containing 3% hydrogen peroxide and 1.5% potassium nitrate. During the process, participants brushed teeth twice dai
Control group:Participants in control group received Crest 3DWhitestrips containing only 3% hydrogen peroxide. During the process, participants brushed teeth twice daily with the given non-fluoride to

Sponsors

The Affiliated Stomatological Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Healthy adults aged 18 to 60 years old who can attend regular follow-up visits during the trial period. 2. Those willing to whiten their teeth and sign the informed consent form. 3. Natural upper anterior teeth 13-23 without intrinsic discoloration such as tetracycline-stained teeth or fluorosis, without extrinsic discoloration such as tobacco stains, plaque or calculus, without untreated dentin hypersensitivity, without fixed orthodontic appliances or removable partial dentures, and without fillings or crown restorations. 4. Agree not to consume foods with extrinsic pigments such as tea, coffee, red wine, and cola during the trial period. 5. Have not used anti-dentin hypersensitivity products and are not participating in other similar trials simultaneously. 6. Agree to postpone any non-emergency dental check-ups and teeth cleaning until the end of the trial. 7. Agree not to use any non-experimental toothpaste or mouthwash during the trial period.

Exclusion criteria

Exclusion criteria: 1.Participants with severe oral diseases, systemic diseases or a history of allergy to the test product; 2.Teeth 13-23 in the progression stage of periodontal disease or having received periodontal treatment (including periodontal surgery) within the past year; 3.Mobility of teeth 13-23 greater than 1 degree; 4.Large fillings on the labial surface of teeth 13-23, suspected of pulpitis, caries, enamel cracks, etc.; 5.Unhealed dentin hypersensitivity in teeth 13-23; 6.Malocclusion of teeth 13-23, wearing fixed orthodontic appliances, fixed dentures or removable dentures, etc.; 7.Teeth 13-23 with intrinsic discoloration such as tetracycline-stained teeth or fluorosis; 8.Smokers; 9.Women in pregnancy or lactation; 10.Currently participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
CIE luminance value L*;CIE red-green degree a*;CIE yellow-blue degree b*;The overall color of tooth color changes ?E*ab;Dental whiteness index ?WID;Cold Air Sensitivity Index;

Secondary

MeasureTime frame
Vita Classical 16-color palette scales;Vita Bleachedguide29 color palette levels;

Countries

China

Contacts

Public ContactYang Deqin

The Affiliated Stomatological Hospital of Chongqing Medical University

500246@hospital.cqmu.edu.cn+86 23 8860 0060

Outcome results

None listed

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