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Clinical Trial Summary

AROMA study is a randomised controlled parallel-group single-site study. Patients randomized in the experimental group benefit from the aromatherapy at their arrival in the operating theatre in the recovery room. 2 drops of essential oils are applied on a compress placed next to the head of the patient. This compress is kept until the patient is leaving the operating theatre. Patients randomized in the control group don't benefit from the aromatherapy. The anxiety evolution is measured in both groups with the Amsterdam Preoperative Anxiety and Information Scale (APAIS). The hypothesis is that aromatherapy alleviate peri operative anxiety during an ambulatory elective upper limb surgery under loco-regional anesthesia.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03583801
Study type Interventional
Source University Hospital, Lille
Contact Cécile RIVOAL, MD
Phone 3.27.14.50.61
Email rivoal-c@ch-valenciennes.fr
Status Recruiting
Phase N/A
Start date September 14, 2018
Completion date September 2023

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