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Control of Pain Due to Dentin Hypersensitivity in Individuals With Molar-incisor Hypomineralization

U

University of Nove de Julho

Status and phase

Unknown
Phase 2
Phase 1

Conditions

Dentin Sensitivity
Molar Incisor Hypomineralization

Treatments

Other: Hygiene Instructions
Procedure: Sealant application
Radiation: Low-level Laser

Study type

Interventional

Funder types

Other

Identifiers

NCT04407702
Hypersensitivity

Details and patient eligibility

About

Background: Dentin hypersensitivity (DH) is defined as high sensitivity of the vital dentin when exposed to thermal, chemical or tactile stimuli. Two mechanisms are required for the occurrence of DH: 1) the dentin must be exposed and 2) the dentinal tubules must be open and connected to the pulp. Molar-incisor hypomineralization (MIH) is a qualitative abnormality of a genetic origin that affects tooth enamel and, in most cases, is accompanied by DH. The control of tooth sensitivity is fundamental to the successful treatment of MIH.

Objective: The aim of the proposed randomized, controlled, clinical trial is to evaluate the effectiveness of different protocols for the control of DH in patients with teeth affected by MIH.

Methods: One hundred forty patients who meet the inclusion criteria will be allocated to four groups. Group 1 will be the control group (placebo). In Group 2, sensitive teeth will be sealed with Permaseal (Ultradent). In Group 3, sensitive teeth will receive low-level laser (LLL) (AsGaAl) at a wavelength of 780 nm (Laser XT Therapy, DMC, São Carlos, SP, Brazil). In Group 4, sensitive teeth will be treated with both LLL and Permaseal (Ultradent). DH will be evaluated 15 min after the application of the treatments and the patients will be reevaluated one week, one month, three months and six months after the treatments.

Discussion: This study will enable the determination of differences in the effectiveness of the proposed treatments as well as differences among the evaluation times for each proposed treatment.

Enrollment

140 estimated patients

Sex

All

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age between 18 and 35 years;
  • Good overall health;
  • At least one tooth with MIH and DH reported in the cervical region with sensitivity equal to or greater than 4 on the VAS.

Exclusion criteria

  • Active caries or defective restorations on the tooth to be analyzed;
  • Sufficient dentin loss that requires restorative treatment or periodontal surgery;
  • Having undergone any professional desensitizing treatment in the previous six months;
  • Having used a desensitizing paste in the previous three months;
  • Use of anti-inflammatory drugs or analgesics at the time of recruitment;
  • Currently pregnant or nursing.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

140 participants in 4 patient groups

Control Group
Experimental group
Description:
The volunteers in this group will receive the same hygiene instructions as the other groups and will undergo both treatments, except that water will be used instead of the sealant and the laser device will be set to a power of 0 W. In other words, the same irradiation procedure will be performed but without the emission of light.
Treatment:
Other: Hygiene Instructions
Sealant Group
Experimental group
Description:
The volunteers in this group will receive treatment with sealant (Permaseal - Ultradent), which is a photopolymerizable methacrylate-based resin.
Treatment:
Procedure: Sealant application
Other: Hygiene Instructions
Low-Level Laser Group
Experimental group
Description:
The volunteers in this group will receive irradiation with AsGaAl laser at a wavelength of 780 nm (Laser XT Therapy, DMC, São Carlos, SP, Brazil) with relative isolation.
Treatment:
Other: Hygiene Instructions
Radiation: Low-level Laser
Low Level Laser + Sealant Group
Experimental group
Description:
The volunteers in this group will receive the same irradiation administered to Low-level Laser Group. During the last session, these volunteers will also receive the same sealant applied in Sealant Group.
Treatment:
Procedure: Sealant application
Other: Hygiene Instructions
Radiation: Low-level Laser

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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