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Clinical study of the frequency of prophylaxis based on the concept of periodontal health

Clinical study of the frequency of prophylaxis based on the concept of periodontal health

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076378
Enrollment
Unknown
Registered
2023-10-07
Start date
2021-07-28
Completion date
Unknown
Last updated
2023-10-09

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

Conditions

Gingivitis

Interventions

Group 1 (Part three):One-on-one personalized oral hygiene instruction based on motivational interviews
Group 0 (Part three):Standard oral hygiene instruction
Observation group (Part two):N/A
Experimental group (Part one):Scaling and polishing

Sponsors

Stomatology Hospital, School of Stomatology, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) 18-70 years of age (this trial is intended to be studied in people of all ages, and volunteers who meet the inclusion criteria of this trial can be included); 2) Good general condition, no serious systemic diseases; 3) periodontal health or only gingivitis; 4) Have 20 or more permanent teeth (except teeth with fixed restorations).

Exclusion criteria

Exclusion criteria: 1) Those who do not meet the diagnostic criteria and inclusion criteria; 2) have received periodontal treatment within the past 6 months; 3) have a habit of smoking; 4) have periodontitis or previous periodontitis; presence of other history of severe periodontal disease; 5) have used antibiotics within 1 month; 6) have removable prostheses or orthodontic appliances in the mouth; 7) have systemic risk factors that affect periodontal health, such as diabetes (people who have typical symptoms of diabetes and meet any of the following conditions: blood glucose = 11.1mmol/L (200mg/dl) at any time of the day or fasting blood glucose level= 7.0mmol/L (126mg/dl) or oral glucose tolerance test 2-hour blood glucose level =11.1mmol/L (200mg/dl)), etc.; 8) now take drugs that have an impact on the experimental results, such as anti-epileptic drugs, immunosuppressants, calcium channel blockers, etc.; 9) pregnant and lactating women (the level of sex hormones such as progestogens and estrogen may affect the inflammation of the gingiva, so it needs to be excluded); 10) Patients who are participating in other similar clinical studies

Design outcomes

Primary

MeasureTime frame
Plaque Index;Bleeding on Probing;Gingival Index;Full-mouth Plaque Score(FMPS);

Secondary

MeasureTime frame
Essential Information Questionnaire;Oral Hygiene Habits Questionnaire;Self-Efficacy of Oral Healthcare scale;Oral Health Impact Profile scale (OHIP-14);Corah Dental Anxiety Scale (C-DAS);Living Habits Questionnaire;

Countries

China

Contacts

Public ContactXia Cai

Stomatology Hospital, School of Stomatology, Zhejiang University School of Medicine

cxshidou@zju.edu.cn+86 153 2571 7939

Outcome results

None listed

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