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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03061422
Other study ID # CEBC-CU-2017-02-14
Secondary ID
Status Not yet recruiting
Phase N/A
First received February 19, 2017
Last updated February 22, 2017
Start date March 3, 2017
Est. completion date November 30, 2018

Study information

Verified date February 2017
Source Cairo University
Contact howaida f. Fouad, master
Email howaidafakhry@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

36 eligible participants will be randomly divided into three groups (n=12) according to the tested chewing gum (A), where (A1) represents participants exposed to xylitol chewing gum, (A2) represents participants exposed to bicarbonate and xylitol chewing gum and (A3) represents control group where participants are exposed to paraffin pellet chewing. The pH of saliva will be evaluated according to time in relation to the gum chewing (T) where (T0) represent the pH before chewing, (T1) represent 5 minutes after gum chewing at fixed time of the day (in the morning from 10 to 11 am).

Direct benefit of the research to the human volunteer:

It is important for high caries risk patients to decrease caries susceptibility as this will eventually decrease their dental treatments and subsequently the treatment cost.

Scientific value and social benefits:

This study will benefit the dentist as the main goal of a dentist is to prevent rather than cure. Also, it will decrease the restorative work carried out by dentist and save this time for educating more patients about caries prevention methods.

Expected risk to the human subjects:

Allergic reactions due to any of the components of the materials used which is rare to occur.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 36
Est. completion date November 30, 2018
Est. primary completion date October 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- Patients eligible for the trial must comply with all of the following at randomization.

1. Age range from 20-50 years

2. High caries risk patients defined according to American Dental Association (ADA)

3. Acidic baseline saliva pH

4. Systematically healthy

5. Not taking any medication interfering with saliva secretion

6. Subjects who signed informed consent

Exclusion Criteria:

- (1) Subjects who wore orthodontic appliances or removable prosthesis (2) Subjects suffering from any medical or systematic disease (3) Smokers (4) Pregnant females (5) Allergy to any of chewing gum ingredients

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Xylitol
caries prevention chewing gum
xylitol with bicarbonate
caries prevention chewing gum
paraffin
chewing gum

Locations

Country Name City State
Egypt Howaida Fakhry Fouad Giza

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

References & Publications (1)

Ballal RK, Bhat SS, Ramdas SS, Ballal S. Effect of Chewing Bicarbonate-containing Sugar-free Gum on the Salivary pH: An in vivo Study. Int J Clin Pediatr Dent. 2016 Jan-Mar;9(1):35-8. doi: 10.5005/jp-journals-10005-1330. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Salivary pH change will be done by digital pH meter an average of 1 year
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