Nasal Compression Device Study for Epistaxis
Epistaxis Nosebleed
About this trial
This is an interventional treatment trial for Epistaxis Nosebleed
Eligibility Criteria
INCLUSION In order to be eligible to participate in this study, an individual must meet all of the following criteria: Presenting with anterior epistaxis determined as someone with venous bleeding that can be controlled with external compression. Stated willingness to comply with all study procedures and availability for the duration of the study. Male or female, aged at least 18. In good general health as determined by the PI or Sub-I(s). EXCLUSION An individual who meets any of the following criteria will be excluded from participation in this study: Known allergic or hypersensitivity reactions to components of NasaClip or oxymetazoline. Less than 18 years of age. Known pregnancy. Unable to provide informed consent. Subjects who are prisoners or who are in police custody. Identified by the medical team as having an acute exacerbation or poor control of any of the following medical conditions: high blood pressure, heart disease, thyroid disease, diabetes, trouble urinating due to an enlarged prostate. Patients taking MAO inhibitors. Medical instability or need for emergent intervention as determined by on-site medical team.
Sites / Locations
- Next Level Urgent CareRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Standard of Care
Nasal Compression Device
Participants assigned to the standard of care arm will be guided through clearing out clots in the nose (if using oxymetazoline), correct head positioning and how to appropriately hold nasal pressure and +/- oxymetazoline applied by a trained medical provider. No packing material will be inserted into the nares and only external pressure will be applied.
Participants assigned to the nasal compression device arm will be provided with the device package which will include the compression device, nasal sponges, and +/- oxymetazoline nasal spray to apply to the sponges as well as written/graphical assembly and application instructions. Participants will then assemble and apply the device themselves under the supervision of a trained medical provider.