🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Turkey / NCT07714915
Starting soon Not applicable

Different Local Anesthesia Techniques for Mandibular Primary Molar Pulpectomy

NCT07714915 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-08-12
Last updated
2026-08-12

Condition(s) studied

Dental AnxietyPainPulpal Diseases

Investigational drug(s) / intervention(s)

Computer-Controlled Local AnesthesiaConventional Inferior Alveolar Nerve BlockArticaine hydrochloride with epinephrine 1:100,000Computer-Controlled Local Anesthetic Delivery SystemStandard Dental Aspirating Syringe

Computer-Controlled Local Anesthesia: Computer-controlled delivery of local anesthetic for mandibular primary molar pulpectomy.

Conventional Inferior Alveolar Nerve Block: Conventional inferior alveolar nerve block administered with a standard dental syringe for mandibular primary molar pulpectomy.

Articaine hydrochloride with epinephrine 1:100,000: A 4% articaine hydrochloride solution with epinephrine 1:100,000 was used as the local anesthetic solution in both study groups.

Computer-Controlled Local Anesthetic Delivery System: A computer-controlled local anesthetic delivery device was used to deliver the anesthetic solution at a constant, pre-programmed injection rate.

Standard Dental Aspirating Syringe: A conventional dental aspirating syringe was used for manual administration of the local anesthetic solution.

Study summary

This study aims to compare the effects of computer-controlled local anesthesia and conventional inferior alveolar nerve block on dental anxiety and pain in children undergoing pulpectomy of mandibular primary molars. Both anesthesia techniques are routinely used in pediatric dental practice and are considered standard methods of care.

Children aged 6 to 8 years who require bilateral pulpectomy of mandibular primary molars will be included in this split-mouth randomized clinical trial. Each participant will receive both anesthesia techniques during separate treatment sessions. Dental anxiety, pain, and physiological parameters, including heart rate, blood pressure, oxygen saturation, and body temperature, will be assessed before, during, and after treatment using validated pediatric assessment scales and routine clinical measurements.

The findings of this study may help identify the anesthesia technique that provides greater comfort and reduces anxiety and pain during pediatric dental treatment, thereby improving the overall treatment experience for children.

Eligibility

Sex
ALL
Min age
6 Years
Max age
8 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Children aged 6 to 8 years. * Requiring bilateral pulpectomy treatment of mandibular primary molars. * Frankl Behavior Rating Scale score of 3 or 4. * American Society of Anesthesiologists (ASA) Physical Status I. * No known allergy to local anesthetic agents. * No previous experience with dental local anesthesia. * No signs of acute abscess or swelling in the treatment area. * Parent or legal guardian able to provide written informed consent and child willing to participate. Exclusion Criteria: * ASA Physical Status II or higher. * Known allergy or contraindication to local anesthetic agents. * Frankl Behavior Rating Scale score of 1 or 2. * Children receiving psychological or psychiatric treatment. * Physical or intellectual disabilities that could interfere with study procedures. * Previous experience with dental local anesthesia. * Presence of acute abscess, cellulitis, or diffuse swelling in the treatment area.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Recep Tayyip Erdoğan University Merkez Rize Province

More Recep Tayyip Erdogan University Training and Research Hospital trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07714915 on ClinicalTrials.gov ↗ ← All trials in Turkey