Actively Recruiting

Phase 4
Age: 7Years - 11Years
All Genders
Healthy Volunteers
ID07113080

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

Age: 7Years - 11Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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)

Follow-up

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

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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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