Evaluation of Germ kill efficacy of 5 oral hygiene products
- Registration Number
- CTRI/2021/03/032326
- Lead Sponsor
- Dabur India Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Subject able to read, understand and sign an appropriate informed consent form indicating willingness to participate
Subjects of both genders in age group 18 â?? 65 years (both the ages inclusive).
Subjects willing to give their swab samples for analysis.
Subjects willing to follow 12 hr overnight gap of brushing/mouthwash and 4 hr fasting after brushing/mouthwash.
Subjects willing to come for follow up visits at the specified time.
Subjects ready to follow instructions during the study period .
Subjects using toothpastes and mouthwash other than Dabur.
•A known history or present condition of hyper sensitivity to any toothpaste.
•The use of antibiotic, antimicrobial, analgesic medications, mouthwash or desensitizing toothpaste during the previous 1 month.
•Any history of periodontal therapy by surgical interventions.
•Any history of dentine hypersensitivity treatment.
•Orthodontic treatment with ï¬?xed appliances.
•Any removable device such as a removable partial denture or orthodontic retainer.
•The presence of any ï¬?xed appliance, large or defective restorations, cracked enamel,
•History of smoking or smokeless tobacco products.
•Subjects having moderate to severe dentine hypersensitivity.
•Subjects having abnormal frenum attachment.
•Subjects who are pregnant, lactating or nursing.
•Subjects having severe level of calculus and/ tartar.
•Any underlying uncontrolled medical illness including diabetes mellitus, hypertension, liver disease or history of alcoholism, HIV, hepatitis, or any other serious medical illness.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method