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NCT04934969 Clinical Trial

The Adjunctive Use of Lavender and Peppermint Essential Oils

Joint Diseases Clinical Trial

— aromatherapy  

Official title:
The Adjunctive Use of Lavender and Peppermint Essential Oils to Manage Nausea, Pain, and Anxiety in an Adult Orthopedic Population

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04934969
Other study ID # 20190050
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 30, 2021
Est. completion date August 1, 2023

Study information
Verified date April 2024
Source University Hospitals Cleveland Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will use passive inhalation of lavender for discomfort, anxiety and peppermint for nausea following joint replacement and spine surgery

Description:

Following review of records for eligibility and consent obtained during pre op visit subjects will be enrolled in study post op they will validate desire to participate and chose to inhale (2 drops of essential oil on cotton ball in a plastic bag) lavender for discomfort or anxiety or peppermint for GI distress Visual analogue scales will be used to rate discomfort , anxiety and nausea

Recruitment information / eligibility
Status Completed
Enrollment 3
Est. completion date August 1, 2023
Est. primary completion date August 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - elective joint replacement able to read and speak English and describe study procedures Exclusion Criteria: pregnancy - unable to smell, sensitivity to fragrances asthma or breathing problems have smoke or vaped in last 2 weeks if atrial fibrillation history no peppermint uncontrolled hypertension above 160/100 non employees of UH or students of CWRU

Study Design

Related Conditions & MeSH terms

Intervention

Dietary Supplement:
• Adjunctive use of lavender and peppermint essential oils
passive inhalation aromatherapy following joint surgery

Locations
Country Name City State
United States University Hospitals of Cleveland Cleveland Ohio

Sponsors (1)
Lead Sponsor Collaborator
University Hospitals Cleveland Medical Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary discomfort, anxiety, or GI distress visual analog sale total of 90 minutes
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