Effect of Starpen Injection Device Versus Conventional Syringe During Anesthesia and Extraction o… (NCT07156032) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effect of Starpen Injection Device Versus Conventional Syringe During Anesthesia and Extraction of Primary Molars
38 participantsStarted 2026-01
Plain-language summary
To evaluate the effect of Starpen device on pain perception during anesthesia and extraction of maxillary primary molars.
Who can participate
Age range6 Years – 8 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Children aged 6-8 years
* Cooperative children ( rating 3 or 4 based on the Frankl behavior scale )
* Medically fit children (ASA I )
* Children mentally capable of communication
* First dental visit
* Patient requiring extraction of upper primary molars due to root caries , crown fractures, periapical disease and failed pulpotomies
* No acute dental pain
Exclusion Criteria:
* Children with a behavioral management problem
* Parental refusal of participation
* Children with previous history of local anesthesia injection
* Medically unfit children (other than ASA I )
* Uncooperative children ( other than Frankl 3,4)
* Children under medications ( antibiotics and analgesics ) for the previous 48 hours that could alter the pain perception
* Teeth that showed any signs of mobility , ankylosis or root resorption affecting more than one third the root
* Acute dental pain