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Clinical verification of Beizhi smart warm-water flosser in auxiliary treatment of periodontitis

Clinical verification of Beizhi smart warm-water flosser in auxiliary treatment of periodontitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062508
Enrollment
Unknown
Registered
2022-08-10
Start date
2022-08-15
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

periodontitis

Interventions

Test I:Designated toothbrush and toothpaste + Beizhi smart warm-water flosser
Test II:Designated toothbrush and toothpaste + Beizhi smart warm-water flosser + Beizhi essence mouthwash

Sponsors

West China Hospital of Stomatology, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 65 years old; 2. The whole body is in good health and has no serious systemic diseases; 3. Patients with at least 20 natural teeth (excluding third molars) in the mouth; 4. Stage I or II periodontitis patients with periodontal probing depth >=3 mm and <=5 mm; 5. Voluntarily participate in the trial, comply with the requirements of the clinical trial, and follow up on time.

Exclusion criteria

Exclusion criteria: 1. Patients addicted to smoking; 2. Patients with dentures or orthodontic devices; 3. Those who have undergone periodontal treatment or scaling treatment in the past 3 months; 4. People with allergies, such as those who are allergic to plastics and other materials; 5. Pregnant and lactating women; 6. Patients who have used tooth whitening or oral cleaning aids (such as electric toothbrushes, dental floss, interdental brushes, etc.) within the past 3 months; 7. Patients who are using or have used hormones or antibiotics within the past 6 weeks; 8. Patients with serious primary diseases such as cardiovascular, liver, kidney, hematopoietic system, and neuropsychiatric diseases; 9. Patients with open dental caries or mucosal lesions or oral soft and hard tissue tumors; 10. The subject has participated in other clinical trials at the same time and has not reached the clinical endpoint; the subject has participated in other clinical trials in the past 3 months; 11. Subjects deemed unsuitable by the investigator.

Design outcomes

Primary

MeasureTime frame
Bleeding on probing;Periodontal probing depth;

Secondary

MeasureTime frame
Plaque index;Clinical attachment loss;Subject satisfaction after intervention;Gingival index;

Countries

China

Contacts

Public ContactXu Xin

West China Hospital of Stomatology, Sichuan University

xin.xu@scu.edu.cn+86 13880603211

Outcome results

None listed

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