Comparison Of Two Methods In The Treatment Of Epistaxis
- Conditions
- Epistaxis.Haemorrhage from nose Nosebleed
- Registration Number
- IRCT201201078640N1
- Lead Sponsor
- Shahid Sadoughi University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria: For Patient Is Admitted With Complaints Of Epistaxis, And Must Have Active Bleeding At The Time Of The Study. Age Older Than 16 Years. Epistaxis Must Be Anterior Type. Exclusion Criteria Were Bleeding Caused By Trauma Or Surgical Procedures. Anticoagulants Drugs Or Bleeding Disorders In Patients (Platelet Count Less Than 100,000, Hemophilia, INR Greater Than 1.5, Hematologic Malignancies), Intervention To Control Bleeding During 6 Months Ago (Cautery, Tampons, Local Treatment). Posterior Epistaxis. Hemodynamic Instability. Upper Respiratory Tract Infection. Accompanied By A Significant Other Complaints (Eg, Chest Pain). Lack Of Patient Consent To Participate In The Study. Deviation Of The Nasal Septum.
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Resolve Bleeding. Timepoint: 15 minutes later. Method of measurement: Direct Inspection.
- Secondary Outcome Measures
Name Time Method ENT specialist consult. Timepoint: At discharge time. Method of measurement: Case inspection.;Patient satisfaction. Timepoint: At discharge time. Method of measurement: upon likert scale.;Need for more intervention. Timepoint: at discharge time. Method of measurement: case inspection.;Recurrenc of epistaxis. Timepoint: 24 houres after discharge from emergency unit. Method of measurement: Interview with patient.;Care duration in emergency unit. Timepoint: After discharge. Method of measurement: Since the establishment of emergency cases until discharge in minutes.