Comparison of the effect of CPP-ACPF and propolis in the treatment of dentin sensitivity

Phase 2

Recruiting

• Conditions: Dentin hypersensitivity.; Other specified diseases of hard tissues of teeth; K03.89

• Registration Number: IRCT20120901010703N4
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 November 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Patients referred to the general and specialized periodontics department of Isfahan Dental School have at least 2 teeth with complaints of cervical dentin sensitivity and sensitivity to cold stimuli that are not adjacent to each other
Patients should be available for three months during the study period and sign the informed consent form
Teeth do not need restorative treatment
People over 18 years old

Exclusion Criteria

Erosion, abrasion, attrition, crack and pulpitis, chronic disease and periodontal disease
Existence of active caries, restored teeth, coronary fractures
Candidate teeth receiving veneers, teeth with ortho braces
People who have received antihistamines, antidepressants, and sedatives in the month before or during the study.
Pregnant and lactating people
smoking
Patients who have used anti-sensitive toothpaste for the past 6 weeks.
Milk protein sensitivity
Sensitivity to benzoate
Improper diet (use of sour and acidic foods)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Amount of patient's pain (dentin hypersensitivity). Timepoint: Before treatment, 15 minutes after treatment in the first session, one week after the first session, two weeks after the first session, one month after the first session, two months after the first session. Method of measurement: Use of cold spray, use of air syringe of unit.