Electronic Anesthetic Efficacy Prof. Ali Rokia Ph.D. Al-Andalus University Prof . Mouetaz Kheirallah Ph.D ArabUST

Mouetaz Kheirallah

Status: Active, not recruiting

Conditions: Pain Perception

Treatments: Drug: control group: therapeutic intervention using a traditional syringe; Drug: Experimental group: Electronic syringe therapeutic intervention arm

Study type: Interventional

Funder types: Other

Identifiers

NCT07257432

ArabUST

Details and patient eligibility

About

A Spilt Mouth Clinical Comparative Evaluation Of The Electronic Anesthetic Efficacy Comparison of traditional local anesthesia with electronic local anesthesia in terms of the ability to reduce pain during injection and the duration of the anesthetic effect

Full description

Study Design:

The mouth will be split in half using a split mouth study. The lower anterior teeth will be injected with a conventional local anesthetic syringe on one side, and the patient will be injected with an electronic anesthetic syringe on the other side.

The study will be conducted on a sample of volunteers aged 18 to 30 years at the Faculty of Dentistry at Al-Andalus University.

The objectives and procedure will be explained to each group of patients, and informed consent will be obtained from each patient to accept the research procedures.

A 2% non-vasoconstrictor lidocaine local anesthetic will be used for all patients.

Enrollment: 30 patients

Sex: All

Ages: 20 to 30 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:". Age ranged from 20 to 30 years , no menstrual cycle, The participants were not allergic to local anesthetics, had not used medication that would alter pain perception, none of them had not ever experienced Smartject injection before, and none of them were alcoholics or smokers, The participants were not allergic to local anesthetics.

Exclusion Criteria:

allergic to local anesthetics ,females during menstural cycle ,bad oral care.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Double Blind

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30 participants in 2 patient groups

Electronic syringe therapeutic intervention arm

Experimental group

Description:

During the appointment, the subjects randomly received 1.8 ml of 2% plain lidocaine for the Intraoral Mental nerve block on both sides (experimental and control). A Carpule syringe with an aspiration and short needles 30G were used on the control side, while Smartject was used on the experimental side

Treatment:

Drug: control group: therapeutic intervention using a traditional syringe

Drug: Experimental group: Electronic syringe therapeutic intervention arm

therapeutic intervention using a traditional syringe

Experimental group

Description:

During the appointment, the subjects randomly received 1.8 ml of 2% plain lidocaine for the Intraoral Mental nerve block on both sides (experimental and control). A Carpule syringe with an aspiration and short needles 30G were used on the control side, while Smartject was used on the experimental side

Treatment:

Drug: control group: therapeutic intervention using a traditional syringe

Drug: Experimental group: Electronic syringe therapeutic intervention arm