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Clinical verification of Beizhi smart portable dental flushing device in preventing and treating gingivitis

Clinical verification of Beizhi smart portable dental flushing device in preventing and treating gingivitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038508
Enrollment
Unknown
Registered
2020-09-23
Start date
2020-10-31
Completion date
Unknown
Last updated
2020-11-30

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

Conditions

Gingivitis

Interventions

Test:Designated toothbrush and toothpaste + smart portable toothbrush

Sponsors

West China Hospital of Stomatology, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Subjects who must meet the requirements of items (1)-(5) can be included in the group: (1) aged 18 to 65 years old; (2) Patients with gingivitis with gingival index >=1.0, plaque index >=1.5, and gingival sulcus depth <3mm; (3) There are teeth 16, 21, 24, 36, 41, and 44 in the mouth without residual roots; (4) The whole body is in good health and no serious systemic diseases; (5) Voluntarily participate in the trial, comply with the requirements of the clinical trial, and follow up on time.

Exclusion criteria

Exclusion criteria: Subjects meet one of the following conditions and cannot be included in the group: (1) Patients with periodontal disease with periodontal pocket depth =3mm; (2) Those who have used hormones and antibacterial drugs in the past 6 weeks; (3) Those who have undergone periodontal treatment or denture treatment in the past 6 weeks; (4) People with allergies, such as those who are allergic to plastics and other materials; (5) Pregnant and lactating women; (6) Patients with serious primary diseases such as cardiovascular, liver, kidney, hematopoietic system, and neuropsychiatric diseases; (7) Patients with open dental caries or mucosal lesions or oral soft and hard tissue tumors; (8) 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; (9) Subjects deemed unsuitable by the investigator.

Design outcomes

Primary

MeasureTime frame
Gingiva index;

Secondary

MeasureTime frame
Gingiva bleeding index;Plaque index;Halitosis value;

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 9, 2026