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Comparison of effectiveness of Fluoride containing paint and glue used during braces treatment in reducing and treating initial caries on teeth

Comparison of effectiveness of Fluoride varnish and Fluoride releasing adhesives in prevention and management of multibracket induced white spot lesions: A Randomized Controlled Trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/11/037918
Enrollment
210
Registered
2021-11-10
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K026- Dental caries on smooth surface Health Condition 2: R52- Pain, unspecified

Interventions

Intervention1: fluoride adhesive: fluoride releasing adhesive will be used once for bonding brackets. Control Intervention1: fluoride varnish: fluoride containing varnish will be applied as a single

Sponsors

ICMR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: class I malocclusion with arch length tooth material discrepancy more than 6 mm

Exclusion criteria

Exclusion criteria: patients with hypocalified teeth or dental flourosis endocrine disorders,congenital anomalies

Design outcomes

Primary

MeasureTime frame
To compare the effectiveness of 2 modes of fluoride delivery agents (fluoride varnish and fluoride containing bonding agent) in preventing and reducing the size of lesions, if they developed during the fixed orthodontic treatment. 2. To compare the results of the 2 above mentioned fluoride delivery modes, with that of the control group. 3. To assess participant related outcomes, such as perception of WSLs and adverse effects due to the 2 agents. Timepoint: Time in months 1-4 months Training of research associate and enrollment of patients 5-30 months:Implementation of project :rendering treatment to patients 31-36 months Data Analysis and compilation of result

Secondary

MeasureTime frame
To assess participant related outcomes, such as perception of WSLs and adverse effects due to the 2 agents.Timepoint: Time in months 1-4 5-30 months 31-36 months Training of research associate and enrollment of patients Implementation of project :rendering treatment to patients Data Analysis and compilation of result

Countries

India

Contacts

Public Contactpanchali batra

Faculty of Dentistry, Jamia Millia Islamia

pbatra@jmi.ac.in

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 21, 2026