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

D

Deraya University

Status and phase

Completed
Phase 1

Conditions

Gingivitis

Treatments

Drug: Yarrow and moringa mixture

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

40 patients

Sex

All

Ages

25 to 55 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

Intervention group
Experimental group
Description:
Bucco-adhesive films with Yarrow and Moringa extract nanoparticles
Treatment:
Drug: Yarrow and moringa mixture
control group
Active Comparator group
Description:
Cholorohexiden oral gargles
Treatment:
Drug: Yarrow and moringa mixture

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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