Inhaled Lavender Oil, Rosemary Oil, and Their Combination in Reducing Dental Anxiety and Pain in Pediatric Dental Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-9
SponsorAlexandria University

About this trial

Background: Dental anxiety and pain are common concerns in pediatric dentistry. These issues can lead to negative experiences for children and can make it difficult for them to cooperate during treatment. While medications can help manage these symptoms, it can also have side effects. This highlights the need for safe and effective complementary treatments. Aromatherapy, particularly with lavender and rosemary oils, has demonstrated anxiolytic and analgesic properties in different fields. However, their effect in helping children cope with dental anxiety and pain during procedures requiring local anesthesia has not yet been thoroughly studied.

Purpose: This study aims to investigate the efficacy of inhaled lavender oil, rosemary oil, and their combination in reducing dental anxiety and pain in children receiving local anesthesia for extraction of lower primary molar

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Frankl behavioural rating score 2 or 3 during preoperative assessment.

Healthy children ASAI.

Children without a previous dental history.

Children presenting with at least one mandibular molar indicated for extraction. (43)

Disqualifiers

Children with colds, asthma, and any other respiratory diseases.

Children who took NSAIDs or analgesic drugs in the last 8 hours before treatment.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Lavender group

    Other intervention

    Children in this group will be inhaled 0.5 ml of prepared mixture (of Lavandula Angustifolia+ Sweet Almond carrier oil ) on a cotton pad attached to the facial steamer .

  • Rosemary group

    Other intervention

    Children in this group will be inhaled 0.5 ml of prepared mixture (of Rosmarinus Officinalis + Sweet Almond carrier oil ) on a cotton pad attached to the facial steamer

  • Combination of both lavender and rosemary

    Other intervention

    Children in this group would be inhaled 0.5 ml of prepared mixture (of Lavandula Angustifolia and Rosmarinus Officinalis + Sweet Almond carrier oil) on a cotton pad attached to the facial steamer .

  • No essential oils

    Other intervention

    Children in this group will be inhaled 0.5 mL of the carrier oil (Sweet Almond ) on a cotton pad attached to the facial steamer .

Treatment groups

80 Participants
are divided into 4 treatment groups
Group A: Group IExperimental treatment 1 intervention
Group B: Group IIExperimental treatment 1 intervention
Group C: Group IIIExperimental treatment 1 intervention
Group D: Group IVActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change in anxiety scores

Venham scale will be used. it ranges from 0 (relaxed) to 5 (Child out of contact with the relaity of threat)

Time frame
up to 1 week

Secondary outcomes

1

Change in anxiety scores (by children)

Comprises a row of five faces ranging from very happy (score 1) to very unhappy (score 5)

Time frame
up to 1 week
2

Change in pain scores

FLACC scale. It is an objectively pain assessment Scale .The scale quantifies pain by observing five distinct behavioral categories: face, legs, activity, cry, and consolability. Each category is assigned a score from 0 to 2, which are then summed to yield a total pain score ranging from 0 to 10.

Time frame
up to 1 week
3

Change in heart rate

it will be used by pulse oximeter.

Time frame
During procedure

Other outcomes

Sponsors and contacts

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