Epistaxis Nosebleed
Conditions
Brief summary
Nosebleeds are very common, occurring in 60% of the population; in some patients, nosebleeds are a life-threatening emergency. To stop a nosebleed in the emergency department, doctors usually have to burn the nose (called cauterization) or insert pledgets (called nasal packing) into the nose to apply direct pressure to the bleeding site. Nasal packing can cause pain and discomfort at the time it is inserted in the nose and again when it is removed. In rare cases it can cause a range of complications: minor complications include scar bands in the nose, but serious complications of nasal packing have also occurred, including death. Nasal packing can also present risks to doctors, such as the risk of contracting airborne and bloodborne infections, like COVID-19 and HIV. Tranexamic acid in pill form or given directly into a vein is a medication that is currently used for nosebleeds. This study looks to evaluate if tranexamic acid in powder form sprayed directly in the nose can be used as an alternative to cauterization or nasal packing for the treatment of nosebleeds.
Interventions
DRUGTranexamic Acid
Tranexamic acid powder intranasally
Sponsors
University of Ottawa
Dr. Anne Conlin
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Capable of giving informed consent form * Stated willingness to comply with all study procedures and availability for the duration of the study * Adults 18 years or older * Male or female * Presenting to the ED with active, spontaneous epistaxis. Anterior versus posterior epistaxis will be identified a priori. Anterior epistaxis is operationally defined as active nasal bleeding that occurs anterior to the anterior limit of the middle turbinate, visible by anterior rhinoscopy.
Exclusion criteria
* Prior sinonasal surgery within the preceding 1 month. * Patients who required medical treatment for epistaxis in the preceding 30 days. * Septum perforation. * Known history of bleeding disorders, including thrombocytopenia, hemophilia, hereditary hemorrhagic telangiectasia, or von Willebrand disease. * History of known thromboembolic disease, including subarachnoid hemorrhage, stroke, or TIA. * Known history of disease of the central nervous system, including seizures, convulsions, or intra-cerebral disease processes/lesions. * Known or suspected history of significant skull base trauma, including skull base fracture or cerebrospinal fluid leak. * Known history of acquired disturbances of colour vision. * Known hematuria or any bleeding related to the kidney. * Pregnant and/or lactating women. * History of known allergy or sensitivity to the study medication. * Presence of signs or symptoms of concomitant emergent conditions, including myocardial infarction, stroke, major trauma, shock, or hemodynamic instability. * Patients with other medical conditions including cognitive limitations or impairment due to substance abuse. * Patients with any other condition that, in the opinion of the investigator, may present an unreasonable risk to the patient, may make the patient unreliable, or may interfere with the study assessments. * Current participation in another interventional clinical trial.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Cessation of epistaxis | Day 1 | Number of participants for whom epistaxis ceased after treatment |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Time to cessation of epistaxis | Day 1 | Measured in minutes |
| Pain of the treatment | Day 1 | Participants' perception of pain will be measured using the Visual Analog Scale (VAS), ranging from 0 (no pain) to 10 (worst pain possible). |
| Total time in the Emergency Department | Day 1 | Measured in minutes |
| Number of participants who returned to the Emergency Department for treatment of epistaxis | within the first 24 hours and the first 5 days after treatment | — |
Other
| Measure | Time frame | Description |
|---|---|---|
| Age | Day 1 | — |
| Anticoagulant and/or antiplatelet medication use | Day 1 | — |
| Type of epistaxis | Day 1 | Anterior versus posterior epistaxis |
| Adverse events and/or patient-reported side effects | up to 3 weeks | — |
| Treatment site complications | up to 3 weeks | Participants will be examined for complications, including synechiae or nasal infections |
Countries
Canada
Contacts
Primary ContactAnne Conlin, HBA&Sc, MD, FRCSC
Outcome results
None listed