Evaluation of State and Shade of White Spot Lesions After Using Different Remineralizing Agents (An in Vivo Study)

A

Al-Azhar University

Status

Completed

Conditions

White Spot Lesion

Treatments

Other: Biomimetic remineralizing agent
Other: Resin Modified Glass Ionomer Varnish

Study type

Interventional

Funder types

Other

Identifiers

NCT04671134
581/3287

Details and patient eligibility

About

The aim of the study is to evaluate the effect of Biomimetic remineralizing agent and resin modified glass ionomer varnish on color shade and state of white spot lesions immediately, after 3 months, and after 6 months. (An in vivo study).

Enrollment

20 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients included in this clinical trial were less than 30 years old.
  • Patients with good general health.
  • Patients who will agree to the consent and will commit to follow-up period.
  • Fully erupted anterior teeth with no cavitated lesions.

Exclusion criteria

  • Patients with any systemic disease that may affect normal healing.
  • Patient with bad oral hygiene.
  • Tetracycline or florosis staining.
  • Patients who could/would not participate in all times of follow-up.
  • Untreated periodontal disease was not allowed.
  • Active caries or defective Restorations in 6 anterior teeth.
  • Bleaching history
  • Patients participating in more than 1 dental study.
  • Patient received fluoride varnish before.

Trial design

20 participants in 2 patient groups

Biomimetic remineralizing agent
Experimental group
Treatment:
Other: Resin Modified Glass Ionomer Varnish
Other: Biomimetic remineralizing agent
Resin modified glass ionomer varnish
Active Comparator group
Treatment:
Other: Resin Modified Glass Ionomer Varnish
Other: Biomimetic remineralizing agent

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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