Effect of Starpen CCLAD in Injection and Extraction
ConditionPain Assessment
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-8
SponsorCairo University
About this trial
The present study aims to evaluate the effect of computer-controlled Starpen automatic injection device versus the traditional syringe on pain perception during Injection of nerve block anesthesia and extraction of mandibular primary molars.
Eligibility criteria
Qualifiers
Children aged 6-8 years
Cooperative children (Rating 3 or 4 based on the Frankl behavior scale)
Medically fit children (ASA I).
Children are mentally capable of communication.
Disqualifiers
Children with a behavioral management problem.
Parental refusal of participation.
Children with a previous history of local anesthesia injection.
Medically unfit children (other than ASA I).
Trial design
Treatments tested in this trial
- computer-controlled Starpen Automatic Injection Device
- Traditional Syringe
Treatment groups
66 Participants
are divided into 2 treatment groupsLocations
Sponsors and collaborators
Source ClinicalTrials.gov