A clinical trail to study the effects of three different desensitising toothpastes on dental hypersensitivity

Phase 4

Completed

• Registration Number: CTRI/2015/08/006091
• Lead Sponsor: Self Funded

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 60

Inclusion Criteria

1.The individuals aged 18 to 75 years with a history of dentinal hypersensitivity.

2.Subjects with at least 20 natural permanent teeth and at least two teeth with a VAS score of >= 4.

Exclusion Criteria

1.Teeth with caries, defective restorations, chipped teeth, deep periodontal pockets, periodontal surgery within the previous six months.

2.Subjects with orthodontic appliances or bridge work that would interfere with evaluation will be excluded.

3.Subjects will also be excluded if there was presence of occlusal overload or occlusal adjustment recently made in the tooth to be studied.

4.Subjects who had undertaken treatment with any product that could influence the dentinal hypersensitivity of the patient in the 30 days prior to baseline will be excluded.

5.Subjects will also be excluded if they were allergic to ingredients used in the study or exhibited any gross oral pathology, eating disorders, chronic diseases, pregnancy and lactation.

6.Medically compromised patients.

7.Poor oral hygiene and to failure to comply with protocol.

Study & Design

• Study Type: Interventional
• Study Design: Not specified