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Evaluation of clinical usefulness of Prinia Smile, GC

Evaluation of clinical usefulness of Prinia Smile, GC - Evaluation of clinical usefulness of Prinia Smile, GC

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038199
Enrollment
40
Registered
2019-10-18
Start date
2019-10-21
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Gingivitis and periodontitis

Interventions

Sponsors

Department of Periodontology and Endodontology, Medical and Dental Sciences, Graduate School of Biomedical Sciences, Nagasaki University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Age:Patients who are 20 years of age or older when obtaining consent (2)Gender:Any (3)Hospitalization / Outpatient: Outpatient only (4)Periodontal examination:Patients who have been diagnosed as having moderate or more chronic periodontitis or invasive periodontitis as a result of periodontal examination (5)Patients who have received sufficient explanation for participation in this study, and who have fully understood and consented to the document by their own will. (6)Systemic periodontal disease treatment has not been received in the past, or even if it has been received, plaque control is poor and there is a wide range of recurrence sites. (7)There are more than 20 remaining teeth in all jaws. 8)Antibacterial drugs.You have not taken any antibacterial drugs within the past 3 months on the registration date.

Exclusion criteria

Exclusion criteria: (1)Patients with diabetes that cannot be controlled (2)Patients with severe heart disease (3)Patients with severe liver and renal dysfunction (4)Patients taking antibody drugs or anti-inflammatory drugs for autoimmune diseases (5)Other patients who are deemed inappropriate by the research director

Design outcomes

Primary

MeasureTime frame
Check if PCR(Plaque Control Record) 20% was achieved

Secondary

MeasureTime frame
Confirm that no adverse events such as pain occurred

Countries

Japan

Contacts

Public Contactyamashita yasunori

Medical and Dental Sciences, Graduate School of Biomedical Sciences, Nagasaki University Department of Periodontology and Endodontology

yamachanpon@nagasaki-u.ac.jp095-819-7643

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026