Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-12
SponsorAnkara Yildirim Beyazıt University
About this trial
This study aims to compare the effectiveness of intraosseous and infiltration anesthesia techniques administered using a computer-assisted anesthesia device (SleeperOne® 5; Dental HiTec, France) during restorative treatments of permanent first molars affected by Molar-Incisor Hypomineralization (MIH) in children. Clinical effectiveness will be evaluated based on the Visual Analogue Scale (VAS), behavioral pain response, pulse rate , salivary chromogranin A levels, and the need for additional anesthesia.
Eligibility criteria
Qualifiers
Individuals applying to the Department of Pedodontics, Ankara Yıldırım Beyazıt University Faculty of Dentistry,
Systemically healthy individuals,
Individuals without any known allergies,
Children between the ages of 6 and 12 years,
Disqualifiers
None
Trial design
Treatments tested in this trial
- Intraosseous anaesthesia using a computerized system
- Infiltration anaesthesia using a computerized system
Treatment groups
30 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov