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Aromatherapy Using a Nasal Clip After Surgery

Aromatherapy Using a Nasal Clip After Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02189980
Enrollment
300
Registered
2014-07-15
Start date
2014-06-30
Completion date
2016-08-31
Last updated
2016-01-15

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

Conditions

Post-operative Nausea

Keywords

Nausea, Post-operative

Brief summary

The purpose of this follow up study is to determine the duration of action regarding aromatherapy to treat nausea occurring postoperatively.

Detailed description

The primary hypothesis of the study is that post-operative patients who meet eligibility criteria and report nausea and receive a blend of 45% ginger, 25% peppermint, 5% spearmint, and 25% cardamom essential oils while using a nasal clip to facilitate inhalation will have more relief from nausea than those who receive normal saline inhalation using the same delivery system. The secondary purposes of the study is to determine the duration of effectiveness of the essential oil blend as compared to the saline in the relief of post-operative nausea and to investigate the degree of comfort participants report using the nasal clip delivery system for aromatherapy.

Interventions

A blend of 45% ginger, 25% peppermint, 5% spearmint, and 25% cardamom essential oils

OTHERDuration of effectiveness of the essential oil blend

Evidence of effectiveness of tested aromatherapy blend in reducing symptoms of post-operative nausea as measured by patient self-report using Likert-type scale measure immediately to one-day post-operative.

OTHERParticipant comfort using the nasal clip delivery system

Comfort of participants using nasal clip delivery system for aromatherapy will be measured by self-report using Likert-type scale immediately to one-day post-operative.

Sponsors

Wake Forest University Health Sciences
CollaboratorOTHER
Balanced Health plus
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

* 18 years or over * cognitively able to give consent based on nurse's assessment, * having gynecological or other abdominal surgery * not allergic to peppermint, spearmint, cardamom or ginger * not receiving blood thinning medications

Exclusion criteria

* less than 18 years old * unable to cognitively give consent * allergic to ginger, peppermint, cardamom or spearmint. * receiving warfarin (Coumadin) or any antiplatelet drug (heparin, 325 mg Aspirin, clopidogrel (Plavix) or other) or a diagnosis of bleeding diatheses (predisposition to abnormal blood clotting/hemorrhage) will not be included in this study. * all surgeries other than gynecological or abdominal surgery

Design outcomes

Primary

MeasureTime frameDescription
Duration of effectiveness of the essential oil blendImmediately to one-day post-operativeEvidence of effectiveness of tested aromatherapy blend in reducing symptoms of post-operative nausea as measured by patient self-report using Likert-type scale measure.

Secondary

MeasureTime frameDescription
Participant comfort using the nasal clip delivery systemImmediately post-op to one-day post-opComfort of participants using nasal clip delivery system for aromatherapy will be measured by self-report using Likert-type scale.

Countries

United States

Contacts

Primary ContactRonald Hunt, MD
rhunt@balancedhealthplus.com704-604-5031

Outcome results

None listed

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