CClinicalTrials.gg
Status unknownNCT02189980Updated Jan 15, 2016

Aromatherapy Using a Nasal Clip After Surgery

An interventional study of Aromatherapy blend and Duration of effectiveness of the essential oil blend in Post-operative Nausea, sponsored by Balanced Health plus. Status unknown at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-01-15.

Sponsored by Balanced Health plus · Not applicable, Interventional, and Supportive care

The sponsor has not verified this record recently (last verified Jan 2016), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
300
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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

Read the 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.

02

Conditions studied

  • Post-operative Nausea

Keywords

  • Nausea
  • Post-operative
03

In context

Nausea

822 studies on the registry are indexed under Nausea; 104 are open to participants now.

This study's planned enrollment of 300 is above the median of 115 across 703 interventional studies indexed under Nausea.

Browse Nausea studies →

Lead sponsor

This is the only study on the registry with Balanced Health plus as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts 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

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
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
300 participants (estimated)

Study arms

  • Placebo comparator
    Saline & nasal clip

    Saline and nasal clip inhaled post-operatively

    Other: Duration of effectiveness of the essential oil blend · Other: Participant comfort using the nasal clip delivery system

  • Experimental
    Aromatherapy blend & nasal clip

    Aromatherapy blend and nasal clip inhaled post-operatively

    Other: Aromatherapy blend · Other: Duration of effectiveness of the essential oil blend · Other: Participant comfort using the nasal clip delivery system

Interventions

  • OtherAromatherapy blend

    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.

06

What researchers measure

Primary outcomes

  1. Duration 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.

    Time frame: Immediately to one-day post-operative

Secondary outcomes

  1. Participant 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.

    Time frame: Immediately post-op to one-day post-op

07

Study locations

1 of 1 sites recruiting
  • CMC -- University
    Charlotte, North Carolina 28262, United States
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 15, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02189980
Lead sponsor
Balanced Health plus
Collaborators
Wake Forest University Health Sciences
Responsible party
Sponsor
First posted
Jul 15, 2014
Start date
Jun 2014
Primary completion
Aug 2016 (estimated)
Completion
Aug 2016 (estimated)
Last update
Jan 15, 2016

Study contacts

Ronald Hunt, MD
Contact
rhunt@balancedhealthplus.com
704-604-5031
Ronald Hunt, MD
principal investigator · Balanced Health plus

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2016. You cannot join it, but the record below documents what was studied.

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