MedPath

A Clinical Study in Subjects with Dental Hyper-Sensitivity

Phase 4
Completed
Registration Number
CTRI/2018/08/015259
Lead Sponsor
Dabur International Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
30
Inclusion Criteria

1.Subjects of either genders

2.Subjects between age of 18 and 55 (inclusive) years

3.Subjects who are medically/systemically fit

4.Non pregnant females

5.Non-lactating females

6.No history of allergy to oral care consumer products - specifically ingredients of tooth paste

7.Subjects should be a regular user of tooth paste and a tooth brush

8.Subjects willing to give a voluntary written informed consent

Exclusion Criteria

1.Subjects who use mouth washes regularly

2.Subjects with a known history or present condition of hyper sensitivity/allergy to any tooth paste, mouthwash or oral hygiene products

3.Subjects who have used any antibiotic, antimicrobial, analgesic medications, or desensitizing tooth paste during previous 1 month

4.Subjects with partial removable dentures, orthodontic bands, or advanced periodontal disease

5.Subjects with inadequate restorations or untreated dental carries

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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