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RecruitingNCT07299474

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

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

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
184 (estimated)
Sponsor
Cedars-Sinai Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to evaluate the efficacy of lavender aromatherapy in adult patients undergoing awake otolaryngologic procedures in the outpatient clinic setting. The main questions it aims to answer are: * Does lavender aromatherapy help reduce anxiety and/or pain, and improve patient comfort during awake otolaryngologic procedures in the clinic? * Do patients subjectively find aromatherapy relaxing and/or beneficial during the procedure? Researchers will compare lavender aromatherapy to placebo (an odorless liquid) to see if lavender aromatherapy helps improve patient comfort during their awake procedure Participants will: * Have their scheduled procedure performed with lavender aromatherapy or placebo during the duration of the procedure * Take a short, less than 1 minute questionnaire both before and after the procedure, describing their levels of anxiety, pain and subjective impressions of the aromatherapy

Conditions

Interventions

TypeNameDescription
OTHERLavender AromatherapyLavender essential oil on cotton ball, and in aromatherapy diffuser
OTHERPlacebo AromatherapySaline on cotton ball and in aromatherapy diffuser

Timeline

Start date
2025-12-01
Primary completion
2027-01-01
Completion
2028-01-01
First posted
2025-12-23
Last updated
2025-12-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07299474. Inclusion in this directory is not an endorsement.