Clinical Evaluation and Assesment of Ginigivitis Patients Treated by Yarrow Natural Extract in Compare to a Contro Group
NCT ID: NCT06070571
Last Updated: 2023-10-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
40 participants
INTERVENTIONAL
2022-05-20
2023-05-20
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Intervention group
Bucco-adhesive films with Yarrow and Moringa extract nanoparticles
Yarrow and moringa mixture
yarrow and moringa mixture nano particles loaded on buccal film
control group
Cholorohexiden oral gargles
Yarrow and moringa mixture
yarrow and moringa mixture nano particles loaded on buccal film
Interventions
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Yarrow and moringa mixture
yarrow and moringa mixture nano particles loaded on buccal film
Eligibility Criteria
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Inclusion Criteria
* good general health
* can follow instructions
Exclusion Criteria
* evidence of antibiotic use during the 4 weeks prior to the study
* were allergic to personal care/consumer products or their ingredients
25 Years
55 Years
ALL
Yes
Sponsors
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Deraya University
OTHER
Responsible Party
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Principal Investigators
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soad ali, PhD
Role: STUDY_DIRECTOR
faculty of pharmacy, Deraya university
Locations
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Soad A. Mohamad
Minya, Minya Governorate, Egypt
Countries
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Other Identifiers
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3/23
Identifier Type: -
Identifier Source: org_study_id
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