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Clinical Trials/NCT04485312
NCT04485312CompletedNot Applicable

Chance to Avoid New Caries by Adding Chlorhexidine Containing Chemotherapeutic Agent to the Conventional Preventive Protocol for Patients With Special Needs

Cairo University1 site in 1 country22 target enrollmentStarted: July 15, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
22
Locations
1
Primary Endpoint
chance to avoid new caries

Study Overview

Brief Summary

Adolescent Special need individuals are most need of easy forms of antibacterial agents, so in this study, using chemotherapeutic agents like the newly introduced varnish containing chlorhexidine seems to be a quite promising tool for local delivery to patients with special needs . Chlorhexidine is a wide spectrum very effective bactericidal used for years against the oral flora while fluorides are well known with their antibacterial ability. This may be an excellent way to reduce the risk assessment in adolescent special needs patients.

Detailed Description

Participants will be divided into two groups according to the tested regimen, where (A1) represents participants exposed to risk based conventional protocol, (A2) represents participants exposed to chlorhexidine containing varnish and risk based conventional preventive protocol. The study will be carried over a period of 10 months (one academic year), the study will be divided into three phases Phase I: Information of the Cariogram parameters (caries experience, diet content, diet frequency, plaque amount, mutans streptococci, fluoride program, saliva secretion and saliva buffer capacity) will be collected, which will be used to generate the individual caries profile, based on which the participants will be divided into 2 risks groups. Phase II: Risk based preventive program will be implemented including the restorative part. Phase III: At the end of 10 months, caries profile will be generated again

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
13 Years to 18 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Clinical diagnosis of disability like : autism and down syndrome.
  • •Must be able to open his/her mouth for varnish application

Exclusion Criteria

  • •systemically unhealthy patients with fetal diseases
  • •Age below 13 and above 18

Arms & Interventions

caries preventive protocol

Active Comparator

preventive protocol for special needs ( tooth brushing , topical fluoride and mouth wash)

Intervention: preventive protocol (Behavioral)

chlorhexidine varnish added to the caries preventive protocol

Other

chlorhexidine varnish preventive caries protocol for special needs

Intervention: chlorhexidine added to the preventive protocol (Behavioral)

Outcomes

Primary Outcomes

chance to avoid new caries

Time Frame: 10 months

% of the green sector in the cariogram

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Katreen Tawfik

principal investigator

Cairo University

Study Sites (1)

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