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

Comparative evaluation of the effects of CPP-ACPF paste and propolis tooth paste on treatment of dentinal hypersensitivity.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120901010703N4
Enrollment
20
Registered
2020-11-17
Start date
2020-11-21
Completion date
Unknown
Last updated
2020-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dentin hypersensitivity. Other specified diseases of hard tissues of teeth

Interventions

Intervention 1: Intervention group 1: Herbex toothpaste, contains propolis. Brush teeth twice a day for two months. It is produced by Dr. Jahangir Knowledge-Based Pharmaceutical Company. Intervention

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

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

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)

Design outcomes

Primary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNarges Naghsh

Esfahan University of Medical Sciences

n_naghsh@dnt.mui.ac.ir+98 31 1792 2870

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026