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Clinical Trials/NCT03577496
NCT03577496
Completed
Not Applicable

Does Aromatherapy Decrease Postoperative Nausea and Vomiting?

The University of Texas Medical Branch, Galveston1 site in 1 country50 target enrollmentJune 15, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Nausea, Postoperative
Sponsor
The University of Texas Medical Branch, Galveston
Enrollment
50
Locations
1
Primary Endpoint
Decrease incidence of postoperative nausea and vomiting (PONV)
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Aromatherapy has been proven to be effective for treating patients with postoperative nausea and vomiting (PONV) after surgery, but few studies analyze its effect on preventing PONV. Most studies use aromatherapy once patients become nauseous, but this study will address a gap in the literature with relation to the effect of aromatherapy in the prevention of PONV.

Detailed Description

The purpose of this pilot study is to determine if aromatherapy will prevent postoperative nausea and vomiting (PONV). Peppermint aromatherapy will be used preemptively to test for effectiveness, decreased PONV, and the ability to avoid anti-emetics. This study will seek to demonstrate that peppermint aromatherapy is a simple, cost effective way to prevent PONV after anesthesia. By decreasing the need for anti-emetics and incidence of PONV, patients may have a quicker recovery time and experience less side effects from anti-emetics, such as increased sedation. This problem is significant to patients and society as it may demonstrate that the inhalation of peppermint can ease PONV and decrease costs due to anti-emetics, wound dehiscence, and prolonged hospital stay. This study may lead to higher levels of patient satisfaction; if the patients are not nauseated they may be more satisfied with their care.

Registry
clinicaltrials.gov
Start Date
June 15, 2018
End Date
December 15, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Adult surgical patients ages 18 and older.
  • Patients deemed medically stable by their surgery team.
  • Anesthesia and Surgeon faculty approval will be obtained prior to asking the patient for their consent.

Exclusion Criteria

  • Unstable patients, such as ICU patients or intubated patients, pregnant women, and prisoners.
  • Patients with a history of severe PONV or severe delirium on emergence from anesthesia will be excluded.

Outcomes

Primary Outcomes

Decrease incidence of postoperative nausea and vomiting (PONV)

Time Frame: Patients will be monitored for up to one hour after surgery to test effectiveness of peppermint oil at decreasing PONV.

Decreased severity of PONV rating with peppermint aromatherapy

Study Sites (1)

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