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Does Aromatherapy Decrease Postoperative Nausea and Vomiting?

Does Aromatherapy Decrease Postoperative Nausea and Vomiting?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03577496
Enrollment
50
Registered
2018-07-05
Start date
2018-06-15
Completion date
2018-12-15
Last updated
2019-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nausea, Postoperative

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.

Interventions

A cotton ball with three drops of peppermint oil will be waved under the patient's nares.

Sponsors

The University of Texas Medical Branch, Galveston
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

* Minors * 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.

Design outcomes

Primary

MeasureTime frameDescription
Decrease incidence of postoperative nausea and vomiting (PONV)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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026