Epidemiology and treatment of epistaxis

• Conditions: R04.0; Epistaxis

• Registration Number: DRKS00021633
• Lead Sponsor: HNO-Uniklinik Freiburg

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2020-04-29
• Study Start: 2020-05-04
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 673

Inclusion Criteria

stationary treatement, majority

Exclusion Criteria

episatxis as a postoperative complication or traumatic cause; ambulatory treatment, minority

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
What: Primary outcome is the treatment that each patient received.<br>When: This parameter is taken retrospectively.<br>How: Data extraction was performed from in-house-software.<br>

Secondary Outcome Measures

Name	Time	Method
localization of bleeding;<br>risk factors;<br>radiographic findings and corresponding pathologies;<br>complications of epistaxis and treatment;<br>stationary time.