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ACTIVE NOT RECRUITING
NCT04260867
NA

Essential Oils for Electrocautery

Sponsor: Northwestern University

View on ClinicalTrials.gov

Summary

The purpose of this study is to assess whether essential oil aromatherapy could improve or eliminate the smell of burnt flesh from electrocautery and subsequently mitigate patient anxiety and discomfort during dermatologic skin surgery. This is a randomized clinical trial. Approximately 210 electrocautery participants will be randomized to receive sham control/no aromatherapy or aromatherapy. Patients will be asked to complete a questionnaire after completion of the procedure to assess their experience. This study was a pilot study designed to determine the feasibility of this procedure. Subjects currently living in the Chicago metropolitan area and meet inclusion/exclusion criteria will be invited and considered for enrollment.

Official title: Utility of Aromatherapy in Reducing Burnt Flesh Smell, Decreasing Intraoperative Anxiety, and Improving the Patient's Overall Experience During Cutaneous Surgical Procedures: a Randomized Controlled Trial

Key Details

Gender

All

Age Range

19 Years - Any

Study Type

INTERVENTIONAL

Enrollment

111

Start Date

2020-12-22

Completion Date

2025-12

Last Updated

2025-01-31

Healthy Volunteers

Yes

Conditions

Interventions

OTHER

Essential Oil

Those randomized to the treatment group will have containers filled with the essential oil of their choice.

OTHER

No Essential Oil

Those randomized to the control group will then be given empty single-use handheld aromatherapy containers containing no essential oil.

Locations (1)

Northwestern University Department of Dermatology

Chicago, Illinois, United States