Efficacy of Camouflaged Syringe vs Conventional Syringe

NCT ID: NCT03566212

Last Updated: 2018-10-05

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

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-08-13

Study Completion Date

2017-08-30

Brief Summary

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This study evaluates the efficacy of Camouflage syringe vs Conventional syringe in reducing Dental Anxiety and increasing behaviour rating.Half of the participants received local anesthesia using camouflaged syringe, while others received using conventional syringe.

Detailed Description

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Dental anxiety and phobia result in avoidance of dental care. Since the injection itself can be painful, pain reduction procedures warrant continued investigation. Camouflage design deals with the visual impact of the needle and syringe though the tactile sensation remains unaltered. In our study, post treatment anxiety levels in camouflaged syringe was reduced as compared to conventional syringe group and this might be because, patients with low anxiety tend to have high pain thresholds.

Conditions

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Dental Anxiety Behavior

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

local anesthesia is administered by using either camouflaged syringe or conventional syringe and was compared for reduction in anxiety levels in both groups
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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conventional syringe

Individuals requiring local anesthesia for dental treatment were treated in first group by using conventional syringe.

Group Type EXPERIMENTAL

Conventional Syringe

Intervention Type DEVICE

local anesthesia was administered in first group using Conventional syringe

camouflaged syringe

Individuals requiring local anesthesia for dental treatment were treated in second group by using camouflage syringe.

Group Type EXPERIMENTAL

Camouflage Syringe

Intervention Type DEVICE

local anesthesia was administered in second group using Camouflage syringe

Interventions

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Conventional Syringe

local anesthesia was administered in first group using Conventional syringe

Intervention Type DEVICE

Camouflage Syringe

local anesthesia was administered in second group using Camouflage syringe

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* retained teeth,
* badly carious teeth,
* mobile teeth
* requiring a dental procedure under local anesthesia were selected.

Exclusion Criteria

* Mentally challenged children
* those with medical conditions contraindicating the use of local anesthesia and / or surgical procedures
Minimum Eligible Age

3 Years

Maximum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Sneha D. Suwarnkar

OTHER

Sponsor Role lead

Responsible Party

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Sneha D. Suwarnkar

Principal investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Sneha D Suwarnkar, MDS

Role: PRINCIPAL_INVESTIGATOR

Saraswati Dhanwantari Dental College and Hospital, Parbhani

Locations

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Dr Sneha D Suwarnkar

Parbhani, Maharashtra, India

Site Status

Countries

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India

Other Identifiers

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SaraswatiDhanwantari

Identifier Type: -

Identifier Source: org_study_id

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