Actively Recruiting

Phase 4
Age: 7Years - 11Years
All Genders
Healthy Volunteers
NCT07113080

Assessing the Efficacy of Lemongrass and Lavender Aromatherapy in Reducing Dental Anxiety and Pain Associated With Local Anesthetic Injections in Pediatric Dental Patients

Led by Hiba Ahmed Eltayeb · Updated on 2025-08-08

48

Participants Needed

1

Research Sites

36 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to evaluate whether aromatherapy using lemongrass or lavender essential oils can reduce dental anxiety and pain perception in children aged 7-11 years undergoing local anesthetic administration in a pediatric dental setting. The main questions it aims to answer are: Does lemongrass or lavender aromatherapy reduce anxiety levels, as measured by salivary cortisol, in children receiving local anesthesia? Does aromatherapy influence pain perception and physiological stress (heart rate) during the procedure? Researchers will compare a lavender aromatherapy group, a lemongrass aromatherapy group, and a control group without aromatherapy to see if the essential oils have a calming effect that reduces anxiety and pain compared to no intervention. Participants will: Inhale either lavender, lemongrass, or no essential oil (control) for two minutes via nebulizer. Undergo local anesthesia administration for a dental procedure. Provide unstimulated and stimulated saliva samples before and after the procedure for cortisol analysis. Report their pain level using the Wong-Baker Faces Pain Rating Scale. Have their heart rate measured before and after the procedure using a finger-type pulse oximeter.

CONDITIONS

Official 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
  • Frankl behavior rating scale category 3 or 4
  • Signed informed consent and child assent
  • At least one vital primary molar with a deep carious lesion
Not Eligible

You will not qualify if you...

  • Previous dental visits
  • Upper or lower respiratory tract problems
  • History of allergy
  • Currently using any medications

AI-Screening

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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

CONTACT

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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