About this trial
This randomized controlled clinical trial aims to evaluate and compare the effectiveness of lavender essential oil and bitter orange essential oil aromatherapy in reducing dental anxiety and pain in children during the administration of local anesthesia. Children aged 6-12 years undergoing dental procedures requiring local anesthetic infiltration will be randomly assigned to lavender aromatherapy, bitter orange aromatherapy, or placebo (empty inhaler). Dental anxiety will be assessed using pulse rate and blood pressure measurements, while pain will be evaluated using the FLACC behavioral pain scale. The findings are expected to provide evidence on the role of aromatherapy as a non-pharmacological, safe, and cost-effective behavior guidance method in pediatric dentistry.
Eligibility criteria
Qualifiers
Children with the age range of 6-12 years
Any dental procedure that requires injection of local anesthesia.
Cooperative patients.(according to Frankl's classification class 1 and 2)
Parents or guardians willing to participate in the study.
Disqualifiers
Children with complicated systemic disease.
Uncooperative patients. .(according to Frankl's classification class 3 and 4)
Children with severe cognitive impairment or developmental disorders
Children with respiratory tract infections.
Trial design
Treatments tested in this trial
- Lavender essential oil in the inhaler
- Bitter Orange essential oil in the inhaler
- Epmty inhaler (Placebo)