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NCT06070571 Clinical Trial

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

Gingivitis Clinical Trial

Official title:
Clinical Assessment of Antibacterial Anti-inflammatory Activities of Yarrow Moringa Herbal Combinations in Bucco Adhesive Films

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06070571
Other study ID # 3/23
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date May 20, 2022
Est. completion date May 20, 2023

Study information
Verified date September 2023
Source Deraya University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date May 20, 2023
Est. primary completion date December 20, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 55 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Yarrow and moringa mixture
yarrow and moringa mixture nano particles loaded on buccal film

Locations
Country Name City State
Egypt Soad A. Mohamad Minya ??????

Sponsors (1)
Lead Sponsor Collaborator
Deraya University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary antibacterial and anti inflammatory activities scoring of erthymia and pain (no pain=0) and the other end (worst pain=10). two weeks
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