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Clinical Trial Summary

66 Participants will be divided into three groups according to the tested regimen (A), where (A1) represents participants exposed to fluoride toothpaste, (A2) represents participants exposed to regimen including fluoride toothpaste and chlorhexidine mouthwash and (A3) represents participants exposed to regimen including fluoride toothpaste, chlorhexidine mouthwash and MI fluoride varnish. The study will be carried over a period of one year, assessment of cariogram will be done in two visits: first visit (baseline: T0) and second visit (after 3 months: T2). In addition assessment of DMF scores will be done in four visits: first visit (baseline: T0), second visit (after 3 months: T1), third visit (after 6 months: T2) and final visit (after 12 months: T3) to obtain the required data


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04032184
Study type Interventional
Source Cairo University
Contact howaida f fouad, Phd
Phone 00201010008948
Email howaidafakhry@gmail.com
Status Not yet recruiting
Phase N/A
Start date October 1, 2019
Completion date November 1, 2020

See also
  Status Clinical Trial Phase
Not yet recruiting NCT04032210 - The Influence of Preventive Regimens Containing Different Toothpastes on Caries Risk of High Risk Patients: A Randomized Clinical Trial N/A