Actively Recruiting

Phase Not Applicable
Age: 16Years - 30Years
All Genders
Healthy Volunteers
ID07180849

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

Age: 16Years - 30Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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.
Not Eligible

You will not qualify if you...

  • Patient undergoing any antibiotic therapy.
  • Patients with any craniofacial abnormality.
  • Patient with mixed dentition.

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

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

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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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