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Actual aromatherapy product for Postoperative Nausea
N/A
Waitlist Available
Research Sponsored by Inova Health Care Services
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients ≥ 18 years of age admitted to the Surgical Unit who are experiencing an initial episode of nausea status post laparoscopic/ robotic sleeve gastrectomy, and/or laparoscopic/robotic Roux-En-Y (RNY) surgery, and/or revisional bariatric surgery; must be able to read and speak English; able to follow directions; bariatric surgeon is part of Inova Medical Group (IMG) and patient is an inpatient.
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 hours
Awards & highlights
Study Summary
Effects of Aromatherapy on Nausea Levels
Eligible Conditions
- Postoperative Nausea
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 hours
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Visual Analog Scale (VAS) from 0-3
Secondary outcome measures
Total post operative anti-emetic usage
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Actual aromatherapy productActive Control1 Intervention
QUEASEEase quick tab Aromatherapy product 50 % chance of participant receiving based on randomization
Group II: Placebo productPlacebo Group1 Intervention
Placebo product (normal saline) 50% chance of participant receiving based on randomization
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Who is running the clinical trial?
Inova Health Care ServicesLead Sponsor
69 Previous Clinical Trials
22,079 Total Patients Enrolled
Mary Ann Friesen, PhD, RNStudy DirectorIHS
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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