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Effect of surfactant on gingival inflammation

Clinical trial on reducing gingival inflammation with authentic ecological toothpaste

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081617
Enrollment
Unknown
Registered
2024-03-06
Start date
2022-10-16
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

Gingival inflammation

Interventions

Experimental group:Surfactant free toothpaste
Control group:Toothpaste with surfactant added

Sponsors

Tianjin Stomatological Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: ? Age 18-60 years old, male and female, no history of allergies to commercially available oral products; ? Voluntarily participate in the test, can participate in the test review on time and can complete the whole test steps; ? Willing to fill in the informed consent and provide personal medical history; ? No other toothpaste or mouthwash was used during the experiment. ? at least 20 natural permanent teeth (except the third molar) without crown restoration; ?There is dental plaque, the whole mouth average PLI=1.2, gingivitis, the whole mouth average GI=1.2.

Exclusion criteria

Exclusion criteria: ? Patients with serious diseases (judged by the clinical examiner), including but not limited to irregular heart rate, uncontrolled hypertension, diabetes, hepatitis of various causes, kidney failure, and need to use drugs before receiving oral therapy; ? Due to other chronic diseases, the need to take antibiotics, hormones, non-steroidal anti-inflammatory drugs, immunosuppressants, immune enhancers, cytotoxic drugs, cell cycle drugs, painkillers and other drugs or preparations that have effects on the gum and oral mucosa; ? Any mental illness or other illness which may lead to a legal determination of limited capacity; ? Pregnant women (urine test should be performed on women during the preparation of excretion), lactating women and those who plan to become pregnant during the test (according to the information provided by the subjects); ? People who participate in the test of other oral health products; ? Patients with moderate and severe periodontitis, pulpitis and oral mucosal diseases; Patients undergoing dental, periodontal, oral surgery, prosthodontic, dental implant and orthodontic treatment; More than 5 unfilled cavities; Those who received tooth extraction or cleaning or scraping within 1 month; A person with calculus; ? Smokers; ?Starch to toothpaste ingredients such as grain allergy.

Design outcomes

Primary

MeasureTime frame
PLI;

Countries

China

Contacts

Public ContactJian Kang

Tianjin Stomatology Hospital

Jiankkang@sina.cn+86 138 2066 4530

Outcome results

None listed

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