CClinicalTrials.gg
CompletedNCT03098212Updated Mar 18, 2026

Aromatherapy for Reducing Labor Pain

An interventional study of Aromatherapy in Pain, sponsored by Chiang Mai University. Completed. Open to female participants. Per ClinicalTrials.gov, last updated 2026-03-18.

Sponsored by Chiang Mai University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years after the study started (first participant enrolled Mar 2015, registered Mar 2017).
Phase
Not applicable
Study type
Interventional
Enrollment
94
Allocation
Randomized
Sex
Female
01

Study summary

Pregnant women who eligible with inclusion criteria are random to two groups. Aromatherapy group will receive the aromatherapy during labor along with standard pain control.

Non-aromatherapy group will receive standard pain control during labor

02

Conditions studied

  • Pain

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03

In context

Pain

2,219 studies on the registry are indexed under Pain; 917 are open to participants now.

This study's enrollment of 94 is above the median of 70 across 1,904 interventional studies indexed under Pain.

Browse Pain studies →

Lead sponsor

Chiang Mai University is the lead sponsor of 116 studies on the registry; 11 are open to participants now.

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

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Singleton pregnancy
  • Nulliparous
  • 37 complete weeks of gestation
  • Cephalic presentation
  • No emergency obstetric complication
  • In labor

Exclusion criteria

Exclusion Criteria:

  • Medical or obstetric complication preclude vaginal delivery
  • Essential oil allergy
  • Side effect of aromatherapy
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
94 participants (actual)

Study arms

  • Experimental
    Aromatherapy

    Receive essential oil diffuse by Aroma diffuser during labor. Pain score and dose of analgesics drug are recorded

    Other: Aromatherapy

  • No intervention
    Non-aromatherapy

    This group receive pain control by standard of care without essential oil (aromatherapy)

Interventions

  • OtherAromatherapy

    On the day of admission for labor. Pregnant women select type of essential oil. Aroma diffuser is used during labor. Pain score was record during latent, early active and late active phase.

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What researchers measure

Primary outcomes

  1. early active phase pain using Visual Analog Scale

    Visual analog scale used to assess pain during cervical dilate 5-7 cm.

    Time frame: The day of labor

Secondary outcomes

  1. latent phase pain using Visual Analog Scale

    Visual analog scale used to assess pain during cervical dilate 3-4 cm.

    Time frame: The day of labor

  2. late active phase pain using Visual Analog Scale

    Visual analog scale used to assess pain during cervical dilate 8-10 cm.

    Time frame: The day of labor

  3. analgesic drug

    doses of analgesic drug request by pregnant women

    Time frame: The day of labor

07

Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03098212
Lead sponsor
Chiang Mai University
Responsible party
Kuntharee Traisrisilp (Principle investigator, Chiang Mai University) — Principal investigator
First posted
Mar 31, 2017
Start date
Mar 2015
Primary completion
Dec 2016
Completion
Dec 2016
Last update
Mar 18, 2026

Oversight

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

Not currently enrolling

This study is completed, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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