Exposed Hypersensitive Dentin Treated With Fluoride Iontophoresis With Remineralizing Agents
NCT ID: NCT06837779
Last Updated: 2025-02-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ENROLLING_BY_INVITATION
NA
20 participants
INTERVENTIONAL
2024-07-01
2025-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Clinical Efficacy of Using Bioactive Desensitizer Gel
NCT07323693
Efficacy of Fluoride Varnish Containing Xylitol Coated Calcium Phosphate Versus Conventional Fluoride Varnish in Management of Hypersensitivity of Exposed Root Surfaces in Adult Patients
NCT04472182
Hypersensitivity and Color Changes of Bleached Teeth Using Different Remineralizing Agents
NCT04875000
Propolis as a Treatment for Cervical Dentin Hypersensitivity
NCT05588518
Clinical Assessment of Bifluorid 10 vs Varnish Fluoride on The Exposed Hypersensitive Cervical Dentin in Adult Patient
NCT04485299
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
SINGLE_GROUP
TREATMENT
TRIPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Fluoride Iontophoresis with Acidulated Phosphate Fluoride gel
assessmen of iontophoresis effect on flouride ions flush to remineralization of demineralized enamel .The treatment will be assessed and recorded using VAS score immediately after the intervention, 3 months, 6 months and one year later.
Fluoride Iontophoresis with Acidulated Phosphate Fluoride
Application of fluoride gel and activated with Iontophoresis electrical pole
remineralizing agents
All remineralizing agents (Casein phosphopeptides -Amorphus Calcium Phosphate, Nano-hydroxyapatite, and Bioactive glass).
Remineralization with sodium fluoride varnish
CASIN PHOSPHOPEPTIDE AMORPHOUS CALCIUM PHOSPHATE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Fluoride Iontophoresis with Acidulated Phosphate Fluoride
Application of fluoride gel and activated with Iontophoresis electrical pole
Remineralization with sodium fluoride varnish
CASIN PHOSPHOPEPTIDE AMORPHOUS CALCIUM PHOSPHATE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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.
35 Years
60 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Al-Azhar University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mohamed Wakwak
ASSOCITE PROFESSOR OF OPERATIVE DENTISTRY
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Mohamed Wakwak, A
Role: PRINCIPAL_INVESTIGATOR
Alazhar Univeristy
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Faculty of Dental Medicine ,Alazhar Univerisity
Cairo, Cairo Governorate, Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
FDAZUC-REC1009/2074
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.