Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07299474

Efficacy Of Lavender Aromatherapy on Anxiety and Pain Reduction During Awake Otolaryngologic Procedures

Led by Cedars-Sinai Medical Center · Updated on 2025-12-23

184

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Brief Title

Efficacy of Lavender Aromatherapy on Anxiety and Pain Reduction During Awake Otolaryngologic Procedures

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults 18 years or older undergoing awake otolaryngologic procedures in an outpatient clinic
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • Hypersensitivity to fragrances
  • Taking systemic NSAIDs or other systemic pain-relieving medications within the last 48 hours
  • Taking anxiolytics, hypnotics, sedating antihistamines, or antidepressants regularly within the past 4 weeks
  • Pregnant or breastfeeding
  • Participation in another clinical research study within the prior 30 days

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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)

Trial Site Locations

Total: 1 location

1

Cedars-Sinai Medical Center Otolaryngology Clinics

Los Angeles, California, United States, 90048

Actively Recruiting

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Research Team

D

Dhruv S Kothari, MD

A

Ankona Ghosh, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Mind-Body Therapies in the Management of Otolaryngologic Disease: A State-of-the-Art Review of Randomized Controlled Trials.

Dhruv S Kothari, Chad A Nieri, Zachary G Tanenbaum...

https://pubmed.ncbi.nlm.nih.gov/37712305

The Efficacy of Lavender Aromatherapy in Reducing Preoperative Anxiety in Ambulatory Surgery Patients Undergoing Procedures in General Otolaryngology.

Michael Wotman, Joshua Levinger, Lillian Leung...

https://pubmed.ncbi.nlm.nih.gov/29299520