Efficacy of Low Level Laser Therapy on İnjection Pain

NCT ID: NCT04243811

Last Updated: 2020-05-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2020-11-15

Study Completion Date

2021-08-15

Brief Summary

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The purpose of this study was to compare the pain during needle insertion and injection in supraperiosteal anesthesia with either topical anesthesia (control) or LLTT (experimental).

Detailed Description

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Conditions

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Pediatric Anesthesia Low Level Laser Theraphy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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laser group

local anesthesia applyed with 940 nm diode laser

Group Type EXPERIMENTAL

Diode Laser

Intervention Type DEVICE

LLLT with dental needle for local anesthesia during dental treatment

conventional group

local anesthesia applyed with topical anesthesia

Group Type ACTIVE_COMPARATOR

topical anesthesia

Intervention Type OTHER

topical anesthesia with dental needle for local anesthesia during dental treatment

Interventions

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Diode Laser

LLLT with dental needle for local anesthesia during dental treatment

Intervention Type DEVICE

topical anesthesia

topical anesthesia with dental needle for local anesthesia during dental treatment

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

In need of treatment of right and left molar teeth of maxilla,

* Does not have any systemic disorder,
* High level of communication that can provide logical answers to the questions we ask
* With parental consent,
* Volunteers who want to participate in the research
* 6-12 years old patients who are compatible with routine dental treatments in the pediatric clinic

Exclusion Criteria

* No need for treatment of right and left molar teeth of maxilla,
* Has a systemic condition
* Low level of communication that cannot provide reasonable answers to the questions we ask
* Without parental consent
* Do not want to participate voluntarily in the research
* Do not attend a check-in
* Patients not in the 6-12 age group
Minimum Eligible Age

6 Years

Maximum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Okan University

OTHER

Sponsor Role lead

Responsible Party

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Sinem yildirim

Assist. Prof. Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Okan University Faculty of Dentistry

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2018/47

Identifier Type: -

Identifier Source: org_study_id

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