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Efficacy of 940 nm diode laser on the treatment of dentin hypersensitivity in periodontal maintenance patients

Efficacy of 940 nm diode laser on the treatment of dentin hypersensitivity in periodontal maintenance patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015102624715N1
Enrollment
45
Registered
2016-05-18
Start date
2016-01-11
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

Dentin hypersensitivity.

Interventions

Intervention 1: In the first group, laser diodide of 940 nm wavelengths with uninitiated 400mm fibers and power 1.5 Watt with continuous radiation mode of two 30 seconds intervals will be used. Inter
Treatment - Other
Treatment - Drugs
Placebo
In the first group, laser diodide of 940 nm wavelengths with uninitiated 400mm fibers and power 1.5 Watt with continuous radiation mode of two 30 seconds intervals will be used.
In secound group(positive control), potassium fluoride gel 2% will be used.
In placebo group, both laser and potassium fluoride gel 2% will be placebo

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
22 Years to 57 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: individuals who have passed first phase of periodontal treatments and have dentin hypersensitivity in teeth with no caries, fracture; any clear tooth crack, fillings and periapical lesion, which will respond to both air and tactile stimuli application tests. Exclusion criteria: individuals with systemic diseases; allergy to materials used in the study; smokers; individuals with active periodontal diseases; pregnant and lactating women; patients who have received treatments related to increased tooth sensitivity; teeth with occlusal overload and recent occlusal re-adjustment therapy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Dentin hypersensitivity. Timepoint: The assessments will be recorded immediately following the treatment at minute 15 and in day 2, 7, and 30. Method of measurement: VAS( visual analogus scale).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTahere Pourseyedian

Qazvin University of Medical Sciences

th.1362@yahoo.com+98 28 3335 3061

Outcome results

None listed

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