About this trial
Our objective is to explore the use of methoxyflurane anesthesia as an adjunct analgesic to local anesthesia during in-office otolaryngology procedures in a prospective pilot study. The main outcome of this study will be patient satisfaction with the medication and analgesia. Secondary outcomes will include level of sedation and analgesia, patient-reported post-procedural pain levels, and any reported adverse events.
Eligibility criteria
Qualifiers
Skin lesion excision or reconstruction
Fine or core needle aspiration biopsy
Mucosal biopsy
Laryngeal injection or biopsy
Disqualifiers
Patient unable to complete the post-procedure questionnaire (either due to time constraints, neurocognitive impairment, etc.)
Patients less than 18 years of age
Pregnancy, intended pregnancy, or current breast-feeding
Inadequate patient understanding or lack of cooperation
Trial design
Treatments tested in this trial
- Methoxyflurane anesthesia