The use of the essential oil lavandin to reduce preoperative anxiety in surgical patients.
Rebecca Braden, Susan Reichow, Margo A Halm
https://pubmed.ncbi.nlm.nih.gov/19962101Actively Recruiting
Led by Cedars-Sinai Medical Center · Updated on 2025-12-23
184
Participants Needed
1
Research Sites
52 weeks
Total Duration
Researchers are evaluating whether lavender aromatherapy can reduce anxiety, pain, and improve comfort for adults undergoing awake otolaryngologic (ear, nose, and throat) procedures in an outpatient clinic setting. This study compares lavender aromatherapy to a placebo to see if patients feel more relaxed or comfortable during their procedure. The trial is sponsored by Cedars-Sinai Medical Center and includes adults aged 18 and older. Participants will be randomly assigned to one of two groups: one group will receive lavender aromatherapy using lavender essential oil on a cotton ball and diffuser before and during their procedure, while the other group will receive a placebo with an odorless saline liquid presented in the same way. The study is double-blinded, meaning neither participants nor researchers know who receives which treatment during the procedure. During the study, participants will complete brief questionnaires before and after their procedure to rate their levels of anxiety and pain using visual analog and Likert scales. Researchers will also collect subjective impressions of the aromatherapy effect. The main outcomes focus on changes in anxiety and pain measured immediately after the procedure, with safety and comfort monitored throughout. Total study participation includes the procedure day and short questionnaire assessments.
CONDITIONS
Efficacy of Lavender Aromatherapy on Anxiety and Pain Reduction During Awake Otolaryngologic Procedures
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Duration of the procedure
Participants receive either lavender aromatherapy or placebo aromatherapy prior to and during awake otolaryngologic procedures to evaluate effects on anxiety and pain reduction.
1 procedure visit (in-person)
Total: 1 location
1
Cedars-Sinai Medical Center Otolaryngology Clinics
Los Angeles, California, United States, 90048
Actively Recruiting
D
Dhruv S Kothari, MD
A
Ankona Ghosh, MD
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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