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Peppermint and Lavender Essential Oil for Nausea
N/A
Waitlist Available
Led By Lorraine Mack, MSN
Research Sponsored by Central DuPage Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
All outpatient Oncology patients > 18 years of age Non pregnant Not cognitively impaired English speaking only Patients who report nausea and/or anxiety
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediately upon completion of the patient's infusion
Awards & highlights
Study Summary
This trial will use peppermint and lavender essential oils to see if they can help with chemotherapy side effects like nausea and anxiety.
Eligible Conditions
- Nausea
- Anxiety
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ immediately upon completion of the patient's infusion
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediately upon completion of the patient's infusion
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Post Intervention Interview From
Trial Design
1Treatment groups
Experimental Treatment
Group I: Peppermint and Lavender Essential OilExperimental Treatment1 Intervention
Young Living Essential oil of Peppermint and Lavender will be used to patients who meet the inclusion criteria.
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Who is running the clinical trial?
Central DuPage HospitalLead Sponsor
13 Previous Clinical Trials
3,405 Total Patients Enrolled
Lorraine Mack, MSNPrincipal InvestigatorCentral DuPage Hospital
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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