Actively Recruiting
The Effect of Lemongrass and Lavender Aromatherapy on Dental Anxiety and Pain Perception in Children Undergoing Local Anesthetic Administration: A Randomized Clinical Trial
Led by Hiba Ahmed Eltayeb · Updated on 2025-08-08
48
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating whether aromatherapy with lemongrass or lavender essential oils can reduce dental anxiety and pain in children aged 7 to 11 years undergoing local anesthetic injections in a pediatric dental setting. The study aims to measure anxiety through salivary cortisol levels, pain perception, and physiological stress using heart rate. This clinical trial is randomized and compares lavender aromatherapy, lemongrass aromatherapy, and a control group without aromatherapy to assess calming effects in young dental patients. Participants will inhale either lavender or lemongrass essential oil through a nebulizer for two minutes before receiving local anesthesia with 4% articaine and 1:100,000 epinephrine after topical anesthesia is applied. The control group will receive the standard procedure without aromatherapy. The study uses simple randomization with concealed allocation and single blinding of outcome assessors, though participants and operators are not blinded due to the nature of the intervention. Children involved in the study will provide saliva samples before and after the dental procedure to measure cortisol levels. Their pain will be assessed right after anesthesia using the Wong-Baker Faces Pain Rating Scale, and heart rate will be monitored before and after the injection using a pulse oximeter. The researchers will analyze these measurements to evaluate anxiety, pain, and physiological stress. The total study participation includes these assessments during the dental visit, with the main outcome focused on anxiety reduction within 30 minutes after the procedure.
CONDITIONS
Brief Title
Assessing the Efficacy of Lemongrass and Lavender Aromatherapy in Reducing Dental Anxiety and Pain Associated With Local Anesthetic Injections in Pediatric Dental Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children aged 7 to 11 years
- Medically free with no chronic illnesses
- Behavior rating level 3 or 4 according to Frankl scale
- Signed informed consent from parents and child assent
- Have at least one vital primary molar with a deep carious lesion
You will not qualify if you...
- Children who have had any previous dental visits
- Children with upper or lower respiratory tract problems
- Children with a history of allergies
- Children currently using any medications
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single day
Participants inhale either lavender or lemongrass essential oil via nebulizer for 2 minutes prior to local anesthetic administration to assess effects on dental anxiety and pain, or receive no aromatherapy if assigned to the control group.
1 treatment visit (in-person)
Duration - Up to 30 minutes post-procedure
Participants' anxiety levels, pain perception, and heart rate are assessed immediately before and after the local anesthetic procedure to evaluate the effect of the aromatherapy intervention.
Assessments completed during the treatment visit
Trial Site Locations
Total: 1 location
1
pediatric dentistry and dental public health department, faculty of dentistry, Ain shams university, Cairo, egypt
Cairo, Cairo Governorate, Egypt, 11566
Actively Recruiting
Research Team
H
hiba AE suliman, master degree candidate
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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