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Three Different Topically Applied Materials as Non-invasive Treatment of Sensitivity in Permanent Teeth With Molar Incisor Hypomineralization

ConditionDentine Hypersensitivity
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-10
SponsorCairo University

About this trial

This clinical study main goal is to investigate the effectiveness of nano hydroxy apatite crystal varnish and potassium nitrate gel as a non invasive approach in managing Dentin Hypersensitivity in MIH-affected teeth.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Children aged from six to ten years old.

Medically free children according to the history taken from their parents.

Children who are categorized as Class I or II according to the American Society of Anaesthesiologists (ASA).

Children whom their parents accept to comply with the follow-up visits.

Disqualifiers

Children with severe behavioral or emotional disabilities.

Children who received analgesics within the last 24 hours before the procedure.

Patients who are using chlorhexidine-based gels or mouthwashes.

A tooth with signs and symptoms of irreversible pulpitis.

Trial design

Design model

Parallel

Treatments tested in this trial

  • nano hydroxy apatite varnish Intervention (1)

    Drug

    Fygg's professional strength, Fygg, USA

  • Potassium Nitrate Gel

    Drug

    Ultradent UltraEZ Desensitizing Gel, Ultradent Inc., USA

  • Varnishes, Fluorid

    Drug

    DentKist Charm Varnish 5% Sodium Fluoride Varnish

Treatment groups

48 Participants
are divided into 3 treatment groups
Group A: 8.6% nano-hydroxy apatite crystals varnish (Fygg's professional strength, Fygg, USA).Experimental treatment 1 intervention
Group B: Potassium Nitrate (Ultradent UltraEZ Desensitizing Gel, Ultradent Inc., USA).Experimental treatment 1 intervention
Group C: 5% fluoride varnish Control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Dentin Hypersensitivity

Face scale: scores from 0-4. the higher the score the worse the sensitivity

Time frame
Baseline, 15 miutes pot-op, 2 weeks post-op, and 4 weeks post op
2

Dentin Hypersensitivity

chiff Cold Air Blasting Sensitivity Scale: scores from 0-3. The higher the score the worse the sensitivity.

Time frame
Baseline, 15 miutes pot-op, 2 weeks post-op, and 4 weeks post op

Secondary outcomes

1

Oral hygiene

Measured by Plaque Control Record: Percentage.

Time frame
baseline, 2-, and 4- week post-op

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Cairo University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: