Microporous Polysaccharide Hemospheres Epistaxis
Withdrawn before enrolling · Not applicable
Conditions studied: Epistaxis
In brief
The purpose of this study is to compare a new treatment for nosebleeds to the treatment that has been used for many years.
Key facts
- Study ID
- NCT02466464
- Run by
- Emory University
- People needed
- 0
- Starts
- 2015-01-01
- Expected to finish
- 2015-12-31
- Last updated by the study team
- 2017-01-26
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- acute epistaxis who have failed conservative measures (including application of pressure and application of oxymetazoline spray) and for which the Otolaryngology service has been consulted
- must be alert and oriented
- hemodynamically stable with a hemoglobin greater than 9 g/dL
- cooperative
You may not qualify if…
- unable to consent or cooperate
- history of hereditary hemorrhagic telengectasias
- hemophilia
- clotting factor deficiencies
- history of prior surgery for epistaxis control
- nasal trauma
- recent sinonasal surgery
- hemodynamic instability
- posterior bleed (as determined by Ear, Nose, Throat physician)
- visibly bleeding vessel
- allergy to product
- current diabetic ketoacidosis
Where it is running
- Emory University Department of Otolaryngology Clinic — Atlanta, Georgia, United States
Full record on ClinicalTrials.gov
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