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Aromatherapy for Reducing Labor Pain

C

Chiang Mai University

Status

Completed

Conditions

Pain

Treatments

Other: Aromatherapy

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Enrollment

94 patients

Sex

Female

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

94 participants in 2 patient groups

Aromatherapy
Experimental group
Description:
Receive essential oil diffuse by Aroma diffuser during labor. Pain score and dose of analgesics drug are recorded
Treatment:
Other: Aromatherapy
Non-aromatherapy
No Intervention group
Description:
This group receive pain control by standard of care without essential oil (aromatherapy)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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