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Clinical Trials/NCT03370328
NCT03370328
Completed
Not Applicable

Essential Oils to Reduce Post-Operative Nausea and Vomiting

University of Rochester1 site in 1 country143 target enrollmentMarch 12, 2018
ConditionsNausea

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Nausea
Sponsor
University of Rochester
Enrollment
143
Locations
1
Primary Endpoint
Mean change in nausea score
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this study is to determine if aromatherapy (essential oil) is effective at reducing up-set stomach and vomiting after surgery and in reducing the need for up-set stomach medications

Detailed Description

If participants decide to take part in this study, they will be asked to use choose a small nasal inhaler from a bag, open the sealed package, and inhale from the nasal inhaler 3 times, inhaling through the nose and exhaling through the mouth, just prior to entering the operating room. During recovery in the Post-operative acute care unit (PACU), nausea severity will be rated using a 0-3 scale where zero indicates no nausea. If your score is 1-3, participants will be instructed/assisted in using a nasal inhaler 3 times, inhaling through the nose and exhaling through the mouth. After 5 minutes, nausea scores will be collected again and if the score is the same or higher, participants will be asked to use the nasal inhaler again in the same manner as before. If their nausea has not resolved after the second use, they will be give anti-nausea medication that a surgeon ordered. This process will be repeated again whenever you complain of nausea, until they are discharged from the hospital.

Registry
clinicaltrials.gov
Start Date
March 12, 2018
End Date
June 30, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Maxine Fearrington

Staff Nurse

University of Rochester

Eligibility Criteria

Inclusion Criteria

  • post-op surgical patients at least 18 years of age or older
  • the ability to understand and follow directions for use of essential oils
  • the ability to understand and give informed consent to study
  • the ability to understand, read and write English
  • ambulatory or short-stay/23-hour patients

Exclusion Criteria

  • History of any pulmonary disease, including but not limited to: asthma, COPD, OSA, chronic bronchitis, pulmonary and ear, nose, throat (ENT) surgery patients
  • Allergy to any of the ingredients in the essential oils
  • Sensitivity to strong odors

Outcomes

Primary Outcomes

Mean change in nausea score

Time Frame: baseline to 24 hours

Nausea will be score on a scale of 0-3 with zero indicated no nausea.

Study Sites (1)

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