Dental Caries Clinical Trial
Official title:
Grape Seeds Versus Standard Measures for Prevention of Caries Incidence in Young Egyptian Adults: A Randomized Controlled Trial
The objective is to conduct an randomized controlled clinical trial to evaluate the
effectiveness of grape seeds extract mouth wash in comparison with standard caries preventive
measures for the prevention of new carious lesions in high caries risk patients.
This study will be designed to test the alternative hypothesis that using grape seed extract
mouth wash in addition to standard preventive measures will show significant difference over
using standard preventive measures alone in preventing incidence of new carious lesions in
high caries risk patients
Research Question:
In high caries risk patients, will the incorporation of grape seeds extract after using
standard oral hygiene measures be beneficial in reducing caries risk and preventing the
incidence of new carious lesions?
Intervention:
The study will be announced at the Faculty of Oral and Dental Medicine, Future University
campus to encourage interested students to participate in the study.
Interested participants will be screened at Conservative Department clinic for eligibility.
Eligible participants will be assessed using caries risk assessment tool (American Dental
Association caries risk assessment form).
Eligible participants will be randomly divided into three groups 1st group will follow only
standard preventive measures (tooth brushing twice a day with fluoride tooth paste and
inter-dental flossing once daily), 2nd group will use grape seeds extract mouth wash beside
standard preventive measure, and 3rd group will use antimicrobial mouthwash with fluoride
beside standard preventive measure General operative procedures Before starting the study the
eligible participants will undergo scaling and prophylaxis polishing, then any carious
cavity, or defective restoration will be treated and filled with resin composite restoration.
New set of manual brushes and dental floss will be given to the participants, after they are
properly trained for the correct brushing and flossing technique. The participants will be
asked to brush their teeth twice a day with fluoride tooth paste and to clean their teeth
inter-dentally with dental floss once a day every day till the end of the study. All the
participants will undergo scaling and prophylaxis polishing at every recall visit Preparation
of the grape seeds extract mouthwash
- Procedure of preparing Grape Seed Extract:
Grape seeds will be collected from grapes which are available in the market. These seeds will
be dried under sunlight for 2 days, and then these seeds will be grounded with cold pressure
technique. Ground grape seeds (100 gm) will be extracted with ethanol/water ratio of 70:30,
vol/vol, by maceration method under stirring at 45 degree centigrade for 2 hours, then The
extract will be filtered(19).
For the intervention 1 group Beside the standard preventive measures that the participants
will be trained to follow, each patient will be given a bottle of grape seeds extract
mouthwash.
The participants will be instructed to rinse 15 milliliter of the mouthwash twice a day after
breakfast and before bedtime and to retain it in their mouth for one minute before
expectorating it, and not to consume any food or drink for 30 minutes after the use of
mouthwash(12).
For intervention 2 group The participants will be instructed to rinse 15 milliliter of the
mouth twice a day after breakfast and before bedtime and to retain it in their mouth for one
minute before expectorating it, and not to consume any food or drink for 30 minutes after the
use of mouthwash. Participants will repeat this protocol for five days every month until the
end of the study.
For the control group Participants in this group will follow only the standard preventive
measures which is brushing twice a day after breakfast and before bed time and daily flossing
inter-dentally before bed time.
In all study groups if any patient during the period of the study develops any carious
cavity, the affected tooth will be treated immediately and restored with resin composite
restoration.
Outcomes:
Visual inspection to detect presence or absence of new caries lesions will be done according
to World Health Organization guidelines. Caries detection will be carried out after careful
drying of the tooth surface using three-way syringe to facilitate detection of initial enamel
lesions (white spot lesions). Also pits and fissure carious lesions will be detected using
visual and tactile method. (26).
Sample size:
The aim of this study is to assess Incidence of new caries in Grape seeds versus standard
measures for prevention of caries. Based on a previous paper by Zhang 2006(27) the difference
in caries development (reduction by antimicrobial mouth wash) between at least 2 groups is
40%. Using power 80% and 5% significance level the investigators will need to study 22 in
each group. This number is to be increased to a sample size of 26 to compensate for losses
during follow up. Sample size calculation was achieved using PS: Power and Sample Size
Calculation software Version 3.1.2 (Vanderbilt University, Nashville, Tennessee, USA
Recruitment:
Patients will be recruited by (S.K and O.N) from the students of Faculty of Oral and Dental
medicine, Future University as the research is targeting young Egyptian adults, only the
eligible participants will be chosen until reaching the target sample size.
-Baseline data collection: For every patient medical and dental history and caries risk
assessment profile will be obtained. Examination chart will be filled by (O.N)
Outcome data collection:
Visual caries inspection and community periodontal index probe(28) will be used by the
assessor (S.K and E.A) after 3 months, 6 months, 9 months and 1 year to evaluate the presence
or absence of new caries lesions.
Patient retention:
The patient's phone number will be recorded in their charts and before every visit the
patient will receive a reminder call by (O.N). If the patient did not answer, another
appointment will be scheduled within a week.
No harms are expected as the intervention product is natural product and Considered as
(generally recognized as safe) by The FDA (Food and Drug Administration Informed consent The
trial will be explained to the patients by the principle investigator. The researcher will
discuss the interventions and possible harms with patients and obtain written consent (in
Arabic) from the patients willing to participate in the trial. An appendix of the consent
form is attached to the protocol
Post-trial care All patients will complete their treatment by the same operator at the clinic
of the Conservative Department. The participants will be followed up even after the trial
ends (6 months follow up period) to treat patient's complaints and prevent any possible
complications
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