EligibleTrials

Intraosseous vs Infiltration Anesthesia in Molar-Incisor Hypomineralization (MIH) Children

Recruiting · NCT07352813 · Interventional (participants receive a specific treatment) · Lead sponsor: Ankara Yildirim Beyazıt University

View the official record on ClinicalTrials.gov →
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Interventions studied

Infiltration anaesthesia using a computerized systemIntraosseous anaesthesia using a computerized system

What this trial is about

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.

Who can take part

Age range
6 Years to 12 Years
Sex
All (male and female)
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Where it is running

1 location listed.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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