- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03098212
Aromatherapy for Reducing Labor Pain
March 16, 2026 updated by: Kuntharee Traisrisilp, Chiang Mai University
Efficacy of Aromatherapy for Reducing Pain During Labor
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
Study Overview
Study Type
Interventional
Enrollment (Actual)
94
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Singleton pregnancy
- Nulliparous
- 37 complete weeks of gestation
- Cephalic presentation
- No emergency obstetric complication
- In labor
Exclusion Criteria:
- Medical or obstetric complication preclude vaginal delivery
- Essential oil allergy
- Side effect of aromatherapy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Aromatherapy
Receive essential oil diffuse by Aroma diffuser during labor.
Pain score and dose of analgesics drug are recorded
|
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.
|
|
No Intervention: Non-aromatherapy
This group receive pain control by standard of care without essential oil (aromatherapy)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
early active phase pain using Visual Analog Scale
Time Frame: The day of labor
|
Visual analog scale used to assess pain during cervical dilate 5-7 cm.
|
The day of labor
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
latent phase pain using Visual Analog Scale
Time Frame: The day of labor
|
Visual analog scale used to assess pain during cervical dilate 3-4 cm.
|
The day of labor
|
|
late active phase pain using Visual Analog Scale
Time Frame: The day of labor
|
Visual analog scale used to assess pain during cervical dilate 8-10 cm.
|
The day of labor
|
|
analgesic drug
Time Frame: The day of labor
|
doses of analgesic drug request by pregnant women
|
The day of labor
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 1, 2015
Primary Completion (Actual)
December 1, 2016
Study Completion (Actual)
December 1, 2016
Study Registration Dates
First Submitted
March 8, 2017
First Submitted That Met QC Criteria
March 27, 2017
First Posted (Actual)
March 31, 2017
Study Record Updates
Last Update Posted (Actual)
March 18, 2026
Last Update Submitted That Met QC Criteria
March 16, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 3487
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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