ClinicalTrials.gg
Not yet recruitingNCT07773181Updated Aug 19, 2026

Nurse Led Aromatherapy

An interventional study of Aromatherapy in Burns and Scalds, sponsored by KK Women's and Children's Hospital. Not yet recruiting at 1 site in Singapore. Open to participants aged 2 Months to 7 Years. Per ClinicalTrials.gov, last updated 2026-08-19.

Sponsored by KK Women's and Children's Hospital · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
2 Months to 7 Years
Sex
All
01

Study summary

The goal of this trial is to see if aromatherapy in addition to pain medication, will help manage pain in pediatric burn patients during their first burn dressing change. Participants aged 2 months to 7 years old will be randomly assigned to usual care (pain medication only) or to receive aromatherapy in addition to pain medication prior to their first burn dressing change. The main question it aims to answer is:

-Does aromatherapy plus pain medication decrease pain more than pain medication alone for young children receiving their first burn dressing change?

All participants will receive the standard pain medications and have their pain assessed on medication administration (prior to aromatherapy for the intervention group), prior to dressing change (after aromatherapy for the intervention group), and 15 minutes after the dressing change is complete.

Once the final pain assessment is complete, there is no more information needed from participants for the purposes of the study. All participants will continue to follow up in the clinic for the remaining dressing changes as needed.

02

Conditions studied

  • Burns and Scalds

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Keywords

  • aromatherapy
  • burns
  • child
  • infant
03

In context

Burns

905 studies on the registry are indexed under Burns; 164 are open to participants now.

This study's planned enrollment of 100 is above the median of 40 across 663 interventional studies indexed under Burns.

Browse Burns studies →

Lead sponsor

KK Women's and Children's Hospital is the lead sponsor of 137 studies on the registry; 33 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
2 Months to 7 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Seen in outpatient burn center
  • Burns not covering more than 7.5% of body surface area
  • First burn dressing change
  • Second degree burns
  • Scalding, flame, or contact burns

Exclusion criteria

Exclusion Criteria:

  • Allergy/ to essential oils, or any components of the aromatherapy formula
  • Airway/hypersensitivity to fragrances, paint fumes, or turpentine
  • Respiratory conditions (e.g. asthma, reactive airway disease, recent wheezing)
  • Inhalation injury

    1. Thermal injury: Caused by direct thermal damage which affects upper airways resulting in edema, stridor and upper airway obstruction
    2. Chemical injury to airways and lung parenchyma from products of combustion
    3. Systemic poisoning from carbon monoxide and/or cyanide
  • Surgery for burn
  • Infection of burn
  • Burns of the face
  • Burns requiring Acticoat dressing
  • Delayed burns (those that have been previously treated outside of the hospital, but have not healed and require further treatment)
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
100 participants (estimated)

Study arms

  • No intervention
    Control Arm: Usual care
  • Experimental
    Intervention Arm

    Participant will wait in the aromatherapy waiting room for 15 minutes prior to dressing change.

    Other: Aromatherapy

Interventions

  • OtherAromatherapy

    Aromatherapy diffusion is a blend of three essential oils, bergamot mint, patchouli, and sweet orange.

06

What researchers measure

Primary outcomes

  1. Pain score as measured by Face, Legs, Activity, Cry, and Consolability (FLACC) scale with first burn dressing change

    Zero is equivalent to no pain and 10 indicates severe pain

    Time frame: FLACC to be completed upon arrival in burn center (baseline), immediately prior to burn dressing change (preprocedural), and 15 minutes after burn dressing change is complete (postprocedural).

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No — While we are collaborating with another institution for the aromatherapy formula, the patients will be recruited only from our institution, therefore IPD does not need to be shared.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Sep 2026; primary completion for Jul 2028, 22 months later.

Of 210 non-industry interventional studies with no phase under Burns, half reached primary completion within 18 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 38. This study's planned 22 months is above that.

Counting every sponsor, half of 239 studies reached it within 15 months; a quarter within 6 and three quarters within 38.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 12, 2026
First posted
Aug 19, 2026
StartEst.
Sep 2026
Primary completionEst.
Jul 2028
CompletionEst.
Jul 2028
Last update
Aug 19, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 19, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07773181
Responsible party
Spiguel Eugenie Ann (Principal Investigator, KK Women's and Children's Hospital) — Principal investigator
First posted
Aug 19, 2026
Start date
Sep 2026 (estimated)
Primary completion
Jul 2028 (estimated)
Completion
Jul 2028 (estimated)
Last update
Aug 19, 2026

Study contacts

Eugenie Spiguel, PhD
Contact
spiguel.eugenie.ann@kkh.com.sg
+65 6225 5554
Joanne Cheng, DNP
Contact
joanne.cheng.sh@singhealth.com.sg
Eugenie Spiguel, PhD
principal investigator · KK Women and Children's Hospital

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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