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Comparing the Antiplaque Efficacy of Titania Nanoparticle Infused Fluoride Varnish vs Conventional Fluoride Varnish in Fixed Orthodontic Patients-A Triple Blind Randomised Controlled Trial
Led by Pakistan Institute of Medical Sciences · Updated on 2025-09-25
20
Participants Needed
1
Research Sites
21 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to compare the antiplaque effects of a novel fluoride varnish infused with titania nanoparticles derived from moringa oleifera leaves extract against a conventional fluoride varnish in patients undergoing fixed multibracket orthodontic treatment. The study focuses on dental plaque accumulation and evaluates the potential benefits of nanoparticle-enhanced fluoride varnishes in dental care. Participants are randomly assigned to one of two groups: Group A receives the conventional fluoride varnish, while Group B receives the fluoride varnish infused with titania nanoparticles. Both varnishes are applied topically to the teeth of fixed orthodontic patients. The study is designed as a triple-blind randomized controlled trial to ensure unbiased assessment. Over six months, researchers will measure the plaque inhibitory effects using a modified plaque index, along with plaque bacterial load and pH levels. Participants will undergo regular dental assessments to monitor these outcomes. The involvement period includes treatment application and follow-up to evaluate differences in plaque accumulation between the two varnishes.
CONDITIONS
Brief Title
Comparing the Antiplaque Effects of Novel Titania Nanoparticle Infused Fluoride Varnish vs Conventional Fluoride Varnish in Fixed Orthodontic Patients.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients planned for fixed orthodontic treatment.
- Patients within age group 16-30 years.
- Patient with no history of previous orthodontic treatment.
- Patients with no active periodontal diseases.
You will not qualify if you...
- Patient undergoing any antibiotic therapy.
- Patients with any craniofacial abnormality.
- Patient with mixed dentition.
AI-Screening
AI-Powered Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 6 months
Participants receive topical application of either conventional fluoride varnish or titania nanoparticle infused fluoride varnish to reduce plaque in fixed orthodontic patients.
Visits scheduled throughout the 6-month treatment period
Trial Site Locations
Total: 1 location
1
Pakistan Institute of Medical Sciences
Islamabad, Pakistan
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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