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Comparison of the effect of two different toothpastes in the treatment of dental hypersensitivity secondary to scaling

Phase 3
Conditions
Dental Hypersensitivity.
Registration Number
IRCT20100412003690N12
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
22
Inclusion Criteria

The patient underwent scaling and Root Planning
The presence of at least 3 teeth with dental hypersensitivity

Exclusion Criteria

History of allergy to toothpaste
Compounds extensive pathology in the oral cavity
Chronic systemic disease
Teeth with tooth sensitivity with more than first degree mobility, teeth with extensive restoration or defect or with prosthetic coating, teeth suspected of pulpitis or with enamel cracking or caries
Pregnant and lactating women
Participants in the study were treated similarly to those who received any dental anti-sensitivity products last month

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The intensity of pain in response to cold, heat and touch stimulants. Timepoint: In the first visit, 15 days later and finally on the 30th day. Method of measurement: Using Visual Analogue Scale.
Secondary Outcome Measures
NameTimeMethod
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