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Dentin Hypersensitivity - Varnish or Laser?

S

Sigmund Freud PrivatUniversitat

Status

Not yet enrolling

Conditions

Dentin Hypersensitivity

Treatments

Device: Laser Irradiation

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Dentin hypersensitivity is a common condition described as a short and sharp pain caused by thermal, evaporative, tactile, osmotic, or chemical stimuli to exposed dentin that cannot be related to another defect or dental pathology. The variety of treatment options and products on the market might seem overwhelming. This study aims to show that laser treatments are efficient in reducing pain scores compared to a desensitizing agent (Gluma). 80 patients with at least two hypersensitive teeth will be enrolled in this study. Patients will be divided randomly into four groups (control group (Gluma), laser group 1 (2.94 µm wavelength), laser group 2 (1064 nm wavelength), laser group 3 (970 nm wavelength)). Visual Analog Scale will be measured before treatment, right after treatment, one week after treatment, one month after treatment, three months after treatment. Mixed Anova's and descriptive analysis will be used for statistical evaluation.

Full description

A total of 80 patients meeting the inclusion criteria will be included in this randomized clinical study. Participants will be randomly divided into four groups. Pain scores will be measured before treatment, right after treatment, 1 month after treatment and 3 months after treatment using the Visual Analog Scala (VAS). Patients will not know which treatment will be performed before nor will the patients from the laser groups know the wavelengths. Pain scores at check-up meetings will be collected by another doctor other than the one who will perform all laser treatments.

Enrollment

80 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • all genders
  • 18-70 years
  • good general health
  • at least two hypersensitive teeth in either jaw
  • initial VAS-score >3

Exclusion criteria

  • Active carious lesions, insufficient restorations, enamel cracks, reversible pulpitis
  • Active periodontal disease, periodontal surgery (in the last 6 months)
  • Bleaching procedure in the last 3 months
  • Analgetic use in the last 72 hours
  • Pregnant/lactating women

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 4 patient groups

Control
Active Comparator group
Description:
Desensitizing Agent Gluma
Treatment:
Device: Laser Irradiation
1. Laser Group
Active Comparator group
Description:
Er:YAG laser
Treatment:
Device: Laser Irradiation
2. Laser Group
Active Comparator group
Description:
Nd:YAG laser
Treatment:
Device: Laser Irradiation
3. Laser Group
Active Comparator group
Description:
970 nm diode laser
Treatment:
Device: Laser Irradiation

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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