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Clinical Trial Summary

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


Clinical Trial 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. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT02189980
Study type Interventional
Source Balanced Health plus
Contact Ronald Hunt, MD
Phone 704-604-5031
Email rhunt@balancedhealthplus.com
Status Recruiting
Phase N/A
Start date June 2014
Completion date August 2016

See also
  Status Clinical Trial Phase
Completed NCT01592708 - Study of Anesthesia Techniques to Reduce Nausea and Vomiting After Jaw Corrective Surgery N/A
Completed NCT01732458 - A Study to Evaluate Aprepitant for the Prevention of Post-Operative Nausea and Vomiting in Children (MK-0869-219) Phase 2