Clinical Evaluation and Assesment of Ginigivitis Patients Treated by Yarrow Natural Extract in Compare to a Contro Group

Deraya University40 enrolled

Overview

A double-blind, prospective, randomized, intra-individual comparative, single-center clinical study was conducted. Participants were placed in parallel groups, and the study was performed in the Department of Operative Dentistry and Periodontology, Dental School and Hospital, Minia university to compare the antibacterial activity of yarrow Moringa herbal combinations nanoparticles in compared to Chlorhexidine as a potential treatment for gingivitis.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Enrollment

Conditions

Gingivitis

Interventions

Yarrow and moringa mixtureDRUG

yarrow and moringa mixture nano particles loaded on buccal film

Eligibility

Sex: ALLMin age: 25 YearsMax age: 55 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * a minimum of four natural uncrowned teeth in one quadrant present * good general health * can follow instructions Exclusion Criteria: * were pregnant or breastfeeding * evidence of antibiotic use during the 4 weeks prior to the study * were allergic to personal care/consumer products or their ingredients

Locations (1)

Soad A. Mohamad

Minya, Minya Governorate, Egypt

Outcomes

Primary Outcomes

antibacterial and anti inflammatory activities

scoring of erthymia and pain (no pain=0) and the other end (worst pain=10).

Time frame: two weeks

Data from ClinicalTrials.gov

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