- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06606587
Effectiveness of the Comfort-In Needle Free Injection System During Palatal Infiltrative Anesthesia
Evaluation of the Effectiveness of the Comfort-In Needle-Free Injector System During Palatal Infiltrative Anesthesia in Children
The goal of this randomized clinical trial is to compare two different injection methods in children. The main question it aims to answer is:
Is the needle-free injection method more painless than the traditional dental method?
Two different methods will be used for children to perform anesthesia for extraction permanent molars.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Meram
-
Konya, Meram, Turkey (Türkiye), 42090
- : Halenur Altan, assoc. prof.
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Child patient between the ages of 6-16, Requiring extraction of maxillary permanent molars and premolars with bilateral palatal infiltration anesthesia, Showing "positive" and "definitely positive" behavior during examination according to the Frankl scale, Family volunteers, No medical or developmental disease
Exclusion Criteria:
If there are medical or developmental disorders, If there is a chronic disease, If there is an allergy to anesthetic solutions, If there is any pathology in the anesthesia area, If the Frankl scale is "negative" and "definitely negative", If the mouth opening is not sufficient, If there is no need for symmetrical treatment in the teeth
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Group Control: Application of Traditional Dental Injection Method
Application of Traditional Dental Injection Method Palatal injection; It was applied 5-10 mm below the palatal gingival margin*, on the attached gum, and with a 45-degree needle angle.
After needle entry, 0.2-0.3
mL of anesthetic solution was stored when bone contact was removed (3-5 mm). 1 mL Articaine Hydrochloride (Ultracaine D-S forte, Hoechst, Canada) containing 1/100,000 epinephrine and a 27 G dental needle were used as local anesthetic agents for injections.
25 patients were included in this group and the procedure was performed.
After waiting for 5 minutes, the anesthetized area was probed with the help of a probe (probing gingiva) to check whether the anesthesia had taken effect.
Afterwards, buccal infiltration anesthesia was performed with the help of a traditional dental injector and tooth extraction was performed.
|
Application of Traditional Dental Injection Method: Traditional Dental Injection method was used for palatal anesthesia of the permanent 1st molar.
|
|
Experimental: Group Experimental: Application of Comfort-in Jet Injection Method
Application of Comfort-in Jet Injection Method Comfort-in jet injection method was used for palatal anesthesia of the permanent 1st molar.
Using a silicone flat cap, it was placed 5 mm below the palatal gingival margin, close to the free gingiva, and with a steep angle.
0.3 ml of anesthetic solution was administered by pressing the jet injection system button.
1 mL Articaine Hydrochloride (Ultracaine D-S forte, Hoechst, Canada) containing 1/100,000 epinephrine was used as a local anesthetic agent in the injections.
25 patients were included in this group and the procedure was performed.
After waiting for 2 minutes, the anesthetized area was probed with the help of a probe (probing gingiva) to check whether the anesthesia had taken effect.
Afterwards, buccal infiltration anesthesia was performed with the help of a traditional dental injector and tooth extraction was performed.
|
Application of Comfort-in Jet Injection Method: Comfort-in jet injection method was used for palatal anesthesia of the permanent 1st molar.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Perception Measured by the Wong-Baker FACES Pain Rating Scale
Time Frame: Immediately after the anesthesia is administered
|
Pain perception was assessed using the Wong-Baker FACES Pain Rating Scale.
The scale ranges from 0 to 10, where 0 represents no pain and 10 represents the worst pain imaginable.
Higher scores indicate greater pain intensity.
|
Immediately after the anesthesia is administered
|
|
Pain Perception Measured by the Face, Legs, Activity, Cry, and Consolability (FLACC) Scale
Time Frame: During the administration of the palatal anesthesia injection.
|
Pain perception was assessed using the Face, Legs, Activity, Cry, and Consolability (FLACC) scale.
The scale ranges from 0 to 10, where 0 indicates no pain and 10 indicates the highest level of pain.
Higher scores indicate worse outcomes (greater pain intensity).
Behavioral responses during the injection were video-recorded and later evaluated.
|
During the administration of the palatal anesthesia injection.
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Halenur Altan, Necmetttin Erbakan University Dentistry Faculty
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- NecmettinEU02
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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