NCT06651827

Brief Summary

This study aims to evaluate the clinical effectiveness of the Er:Cr laser in reducing dentin hypersensitivity (DH), a common dental condition characterized by sharp pain in response to thermal, mechanical, chemical, or osmotic stimuli.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 15, 2023

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2024

Completed
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2024

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

October 19, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

October 22, 2024

Completed
Last Updated

October 30, 2024

Status Verified

June 1, 2023

Enrollment Period

12 months

First QC Date

October 19, 2024

Last Update Submit

October 27, 2024

Conditions

Keywords

Dentin hypersensitivityEr,Cr:YSSG laserYeaple ProbeVisual Analog Scale

Outcome Measures

Primary Outcomes (1)

  • The objective of this study is to evaluate the effectiveness of the Er,Cr:YSGG laser in the treatment of Dentin Sensitivity

    The objective of this study is to evaluate the effectiveness of Dentin Sensitivity using the Yeaple Probe

    Dentin sensitivity was measured using the Yeaple Probe and air stimulation tests before of the Er,Cr:YSGG laser in the and after treatment.

Study Arms (1)

Dentin sensitivity was measured before and after treatment

EXPERIMENTAL

Dentin sensitivity was measured using the Yeaple Probe and air stimulation tests before and after treatment

Diagnostic Test: Dentin sensitivity was measured using the Yeaple Probe and air stimulation tests before and after treatment

Interventions

Dentin sensitivity was measured using the Yeaple Probe and air stimulation tests before and after treatment. The effectiveness of the treatment was assessed at baseline, 30 minutes, 1 week, and 1 month post-treatment using the Visual Analog Scale (VAS) and Yeaple Probe scores.

Dentin sensitivity was measured before and after treatment

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Patients \>18 years old
  • Express a desire for treatment for their dentin hypersensitivity
  • Only sensitive teeth without indications for restorative procedures were considered eligible
  • Informed consent was obtained from all participants

You may not qualify if:

  • \- Patients with underlying systemic conditions or those taking medications that could affect the study outcomes, such as analgesics, anti-inflammatory drugs, or sedatives within 72 hours prior to enrollment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Can Tho University of Medicine and Pharmacy

Can Tho, 900000, Vietnam

Location

Related Publications (2)

  • Haneet RK, Vandana LK. Prevalence of dentinal hypersensitivity and study of associated factors: a cross-sectional study based on the general dental population of Davangere, Karnataka, India. Int Dent J. 2016 Feb;66(1):49-57. doi: 10.1111/idj.12206. Epub 2015 Nov 19.

  • Yilmaz N, Baltaci E, Baygin O, Tuzuner T, Ozkaya S, Canakci A. Effect of the usage of Er,Cr:YSGG laser with and without different remineralization agents on the enamel erosion of primary teeth. Lasers Med Sci. 2020 Sep;35(7):1607-1620. doi: 10.1007/s10103-020-03015-0. Epub 2020 May 29.

MeSH Terms

Conditions

Dentin Sensitivity

Condition Hierarchy (Ancestors)

Tooth DiseasesStomatognathic Diseases

Study Officials

  • Quang Xuan Vo

    Can Tho University of Medicine and Pharmacy

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 19, 2024

First Posted

October 22, 2024

Study Start

June 15, 2023

Primary Completion

June 1, 2024

Study Completion

June 15, 2024

Last Updated

October 30, 2024

Record last verified: 2023-06

Data Sharing

IPD Sharing
Will not share

Locations