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Enrolling by invitation NCT06837779

Exposed Hypersensitive Dentin Treated With Fluoride Iontophoresis With Remineralizing Agents

No phase Interventional Dentin Hypersensitivity

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Fluoride Iontophoresis with Acidulated Phosphate Fluoride, Remineralization with sodium fluoride varnish.
Who it may be relevant to
Registry conditions: Dentin Hypersensitivity. Basic parameters: 35 years — 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Clinical Evaluation of Exposed Hypersensitive Dentin Treated With Fluoride Iontophoresis Application in Comparison With Two Different Remineralizing Agents (a Randomized Clinical Trial)

Overview

The goal of this clinical trial is to learn if the application of fluoride works to treat patients suffering from dentin hypersensitivity. It will also learn about the safety of using fluoride iontophoresis with Acidulated phosphate fluoride gel. The main questions it aims to answer are: Does the remineralizing agent have the ability to decrease dentin sensitivity? Researchers will compare Fluoride Iontophoresis with Acidulated Phosphate Fluoride gel , Casein phosphopeptides-Amorphus calcium phosphate (CPP-ACP), nano-hydroxyapptite (NHAP) and -active glass in decreasing dentin hypersensitivity . Participants will: * Application of remineralizing agent every 3 months * Visit the dental clinic once every 3 months for checkups and tests

Detailed description

Assess the efficacy of fluoride iontophoresis in remineralization in comparison with other ingredients.

Interventions

  • Drug Fluoride Iontophoresis with Acidulated Phosphate Fluoride
    Application of fluoride gel and activated with Iontophoresis electrical pole
  • Drug Remineralization with sodium fluoride varnish
    CASIN PHOSPHOPEPTIDE AMORPHOUS CALCIUM PHOSPHATE

Primary outcome measures

  • Visual Analogue Scale [Time frame: 12 months]

Eligibility criteria

Inclusion criteria

  • Patients within 35-60 years of age.
  • Each patient has 4 or more exposed roots of posterior teeth having sensitivity.
  • Good oral hygiene.
  • Patients who will agree to the consent and will commit to the follow-up period.
  • Patients will follow instructions during study time.
  • Teeth that were vital.

Exclusion criteria

  • Patients with any systemic disease that may affect normal healing.
  • Patient with bad oral hygiene, high caries index and high plaque index
  • Patients participating in more than 1 dental study.
  • Active carious lesions.
  • Intrinsic and extrinsic stains.
  • Any previous filling of selected teeth.
  • Cracked and malformed teeth.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Single group
Masking
Triple blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Faculty of Dental Medicine ,Alazhar Univerisity — Cairo

Identifiers

NCT: NCT06837779 · FDAZUC-REC1009/2074

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗