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Terminated
NCT06316934
Lavender Aromatherapy to Decrease Anxiety/Pain Perception During Office Hysteroscopy
Conditions: Anxiety, Pain, Procedural
Sex: Female
Ages: 18 Years – 99 Years
Healthy volunteers: Yes
Phase: PHASE2
Enrollment: 22
Sponsor: University of Florida
Location: University of Florida Gainesville Florida
Summary
Office hysteroscopy is an invaluable practice to treat a myriad of gynecological processes. However, a limiting factor is the perceived pain and anxiety. In a randomized pilot study, treatment with lavender aromatherapy will significantly decrease the stress/anxiety levels associated with office hysteroscopy, as measured on a visual analogue scale and the Hospital Anxiety and Depression Scale (HADS) questionnaire when compared to control subjects receiving distilled water placebo.
Eligibility Criteria
* Inclusion Criteria:
* Women aged 18 and over
* Scheduled to undergo office hysteroscopy procedure
* Able to give informed consent
* Able to read and write in English
* Anxiety score \> 0 on a numerical scale at baseline
* Exclusion Criteria:
* Any contraindication to office hysteroscopy (active pelvic infection, confirmed cervical or endometrial cancer severe hypertension, or any other condition that might be worsened by an uncomfortable test)
* Allergy to lavender oil, or any of its components
* Withdrawal Criteria
* The patient requests terminating participation
Source: ClinicalTrials.gov (NCT06316934). StuddyBuddy aggregates publicly available trial information.