Clinical efficacy of toothpaste with anticalculus agent

Not Applicable

Recruiting

Conditions: Not Applicable

Registration Number: KCT0003479

Lead Sponsor: AmorePacific

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 80

Inclusion Criteria

Adult men and women aged 18 to 80
-Patients who were found to be active in calculus formation
-Calculus Index 2 or more on the lingual surface of the lower anterior teeth
-Patients who can get proper brushing habits

Exclusion Criteria

-Pregnant or lactating women
-Patients who have taken medicines that cause soft tissue enlargement within 2 weeks of screening (eg, diuretics, immunosuppressants, antagonists) or are probable to be taken during the trial
-Patients with oral skin disease or lesions (eg, erosive lichen planus, erosive squamous cell carcinoma, oralitis, ulcer, malignant tumor)
-Patients with moderate to severe periodontitis
-Patients with systemic disease that have a significant effect on this trial
-smokers more than 1/2 package daily
-Patients with hypersensitivity to the same formulation (including ingredients) in the past
-Patients who are judged to be inappropriate for the judgment of other clinicians

Study & Design

Study Type: Interventional Study

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Clinical index: plaque index (PI), Gingival Index (GI), Calculus Index (CI), Probing Depth (PD), Bleeding on Probing (BOP), Gingival Recession and Clinical Attachment Level

Secondary Outcome Measures