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effect of laser and Propolis in treatment of dentin hypersensitivity

Clinical trial of comparison between Nd:YAG laser and Propolis in treatment of dental sensitivity in patients with dentin hypersensitivity

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016111230858N1
Enrollment
25
Registered
2017-03-23
Start date
2016-03-19
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. Other specified diseases of hard tissues of teeth

Interventions

Intervention 1: laser radiation in cervical area of sensitive teeth in three sessions with one week intervals. Nd:YAG laser with 1064 nanometer wavelength, 1W power, 10 Hz frequency, short pulse mode,
Treatment - Devices
Treatment - Other
laser radiation in cervical area of sensitive teeth in three sessions with one week intervals. Nd:YAG laser with 1064 nanometer wavelength, 1W power, 10 Hz frequency, short pulse mode, 300µm fiber ti
40% Propolis gel applying in cervical area of sensitive teeth in three sessions with one week interval

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: having at least two hypersensitive teeth in two sides of mouth (one right and one left); age of =18 years; vitality of examined teeth; no carious lesions; fractures or cracks and restorations in examined teeth exclusion criteria: patient absent in fallow up appointments; systemic diseases; Pregnancy; periodontal surgery within last 3 months; orthodontic treatment in that same course; desensitizing therapy within last 1 month; existing of pulpitise and crown in examined teeth

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Dentin hypersensitivity. Timepoint: before treatment and immediately after, one week after, two weeks after, one month after and finally three months after treatment. Method of measurement: VAS (visual analog scale).

Secondary

MeasureTime frame
-. Timepoint: -. Method of measurement: -.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Rasti

dentistry collage of Yazd

marasti68@yahoo.com; dr.rasti68@gmail.com+98 35 3625 0344

Outcome results

None listed

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