Clinical Trial

Preemptive Analgesia for Pain and Anxiety Control in Children With MIH

Recruiting
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Record status
This record was last updated January 28, 2026 (before its estimated February 2026 completion). Its status may not reflect the trial's current state.
Summary
This randomized, triple-blinded clinical trial aims to evaluate the effect of preemptive analgesia using ibuprofen on pain perception and anxiety during restorative treatment of first permanent molars in children diagnosed with molar-incisor hypomineralization (MIH). MIH-affected teeth often present with hypersensitivity, difficulty in achieving adequate anesthesia, and increased dental anxiety, which complicates dental treatment. Participants aged 6-12 years with MIH will receive either ibuprofen syrup or placebo 30 minutes before treatment. Pain will be assessed using the FLACC Behavioral Pain Scale and Wong-Baker FACES scale, and anxiety will be evaluated through heart rate and oxygen saturation. The results will determine whether preoperative ibuprofen reduces intraoperative pain and improves anxiety control in this population.
Trial Details
NCT Number NCT07374354
Lead Sponsor October University for Modern Sciences and Arts
Conditions Pain and Anxiety in Children With MIH
Enrollment 46 participants
Start Date 2026-02
Primary Completion 2026-02 (estimated)
Study Completion 2026-02-01 (estimated)
Updated on ClinicalTrials.gov 2026-01-28