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Completed

NCT Number: NCT03577496

Does Aromatherapy Decrease Postoperative Nausea and Vomiting?

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Texas Medical Branch

Galveston, Texas, 77555, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Peppermint oil

Other

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

Primary outcomes

  1. 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

Sponsors and collaborators

Lead sponsor

The University of Texas Medical Branch, Galveston

Other

Registry information

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Jul 5, 2018
Registry last updated
Jan 9, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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