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Clinical Trials/NCT03590977
NCT03590977UnknownNot Applicable

Evaluation the Efficacy of a Herbal Licorice on Reducing Salivary Streptococcus Mutans Levels (A Randomized Clinical Trial)

Cairo University0 sites52 target enrollmentStarted: September 1, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
52
Primary Endpoint
salivary bacterial count

Study Overview

Brief Summary

To compare the effect of a natural herbal licorice containing preventive measure alternative to chlorohexidine preventive measure to decrease the effect of streptococcus mutans.

Detailed Description

A total number of fifty-two patients will be enrolled in the study. They will be divided into two groups: study group and control group. Study group will be subjected to licorice mouthwash and the control will be subjected to chlorohexidine mouth wash. Salivary bacterial count will be evaluated for both groups.

Study Design

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

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •over 18 years old
  • •co-operative patients
  • •not allergic to licorice
  • •not allergic to chlorohexidine

Exclusion Criteria

  • •pregnancy
  • •allergic patients to licorice
  • •allergic patients to chlorohexidine
  • •lack of compliance
  • •evidence of parafunctional habits
  • •patients with periodontal disease
  • •xerostomia
  • •participants that receive any microbial agent two weeks prior to the study

Arms & Interventions

licorice extract mouthwash

Experimental

administration of a mouthwash containing licorice as a preventive measure to high caries risk patients (faculty of pharmacy, cairo university)

Intervention: licorice extract mouthwash (Other)

chlorohexidine mouthwash

Placebo Comparator

administration of chlorohexidine 0.2% in 1:1 diluation mouthwash that is broad spectrum antimicrobial activity to high caries risk patients

Intervention: chlorohexidine mouthwash (Other)

Outcomes

Primary Outcomes

salivary bacterial count

Time Frame: after one week

streotococcus mutans bacterial count

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Nancy Helmy Blamon Mikhael

Assistant lecturer

Cairo University

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