Risk Reduction
Conditions
Brief summary
This study will be conducted to evaluate the effect of Propolis-containing toothpaste in comparison to Fluoride-containing Toothpaste by caries risk assessment in high caries risk patients.
Detailed description
A total of 40 patients will be assigned in this study. Patients will be randomly divided into two groups according to type of Toothpaste (A) where group A1 patients will use propolis containing toothpaste twice daily while group A2 patients will use fluoride containing toothpaste twice daily as control with 20 patients in each group. Each group will be further divided into three groups according to caries risk assessment times (T) where T0 represents caries risk assessment of patients before application of propolis and fluoride toothpastes and T1 represents caries risk assessment of patients after three months of application of propolis and fluoride toothpastes, T2 represents caries risk assessment of patients after six months of application of propolis and fluoride toothpastes. Both Propolis containing toothpaste and fluoride containing toothpaste will be placed in concealed tubes. The tubes will completely wrapped by plain white tape to conceal the formulation of toothpaste. Participants are given the tubes of toothpaste and soft brush with a coloured mark at 2 cm length of the bristle surface. The technique can be summarised in four steps: 1. 2 cm of the toothpaste will be squeezed over the wet toothbrush bristles 2. The upper and lower teeth will be brushed for 2 min; 3. After brushing, the remaining toothpaste foam and saliva slurry will be swished around the dentition with active movements of the cheeks, lips and tongue, forcing the slurry in between the teeth for about 20 seconds before expectorating the slurry 4. No post-brushing water rinsing will be carried out All these steps will be presented in a reminder card and all patients will put a tick mark for every step.
Interventions
DRUGpropolis-containing toothpaste
participants will use propolis-containing toothpaste for 6 months
DRUGFluoride-containing toothpaste
participants will use Fluoride-containing toothpaste for 6 months
Sponsors
Cairo University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Participants should be over 18 years of age. * Participants should be high caries risk. * Systematically healthy. * Not taking any medication interfering with saliva secretion. * Participants who signed informed consent.
Exclusion criteria
* Participants with a compromised medical history. * Participants under systemic disease treatment, with antibiotic, steroid or any medication known to cause dry mouth. * Severe or active periodontal disease. * History of allergies or other adverse reactions to propolis, or oral care product or their ingredient.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Improving caries risk | 6 months | caries risk assessment |
Outcome results
None listed