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Evaluation of the effect of two low level diode lasers 660nm and 810nm in the treatment of dentin hypersensitivity

Evaluation of the effect of two low level diode lasers 660nm and 810nm in the treatment of dentin hypersensitivity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017062022699N4
Enrollment
96
Registered
2017-07-31
Start date
2016-10-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

dental hypersensitivity. Dental examination

Interventions

Intervention 1: Radiation with 660 nm diode lasers with a power of 30 mW in contact and perpendicular to the tooth surface, for 120 seconds, continuous irradiation and returning in four sessions with
Treatment - Other
Placebo
Radiation with 660 nm diode lasers with a power of 30 mW in contact and perpendicular to the tooth surface, for 120 seconds, continuous irradiation and returning in four sessions with a one week inter
Radiation with a low-power 810 nm diode laser with a 100 mW power ,in contact and perpendicular to the tooth surface, for 120 seconds, continuous irradiation and returning in four sessions with a one
In the control group, the teeth were not exposed to laser irradiation, and the direction of blindness of the study group was limited to simulating the conditions under the radiation beam.

Sponsors

Vice Chancellor for research of Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients referring to dental faculty of Isfahan University of Medical Sciences in 1395-96 who have cervical dentin hypersensitivity in at least three teeth in three separate half-jaws. Teeth that are sensitive to cold stimulant testing. Exclusion criteria: Caries, restored teeth, crown fracture, dental cracks, smokers, active periodontal disease, pregnancy, patients who have taken analgesics for 72 hours before the laser treatment, patients who have received anti-Sensitivities toothpaste over the past 6 weeks.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Initial improvement of dental hypersensitivity. Timepoint: At intervals of one week for a month before and after laser radiation. Method of measurement: According to the visual analogue scale.

Secondary

MeasureTime frame
Long-term improvement in dental hypersensitivity. Timepoint: One week, 30 days and 60 days after the last laser radiation session. Method of measurement: According to the visual analogue scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahdi Kachouei

Faculty of Dentistry, Isfahan University of Medical Sciences

birang@dnt.ac.irkachueimk@yahoo.com+98 31 3669 1597

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026