Comparison Of Two Methods In The Treatment Of Epistaxis

Comparison the effect Of Pressure On The Nose By Nose Stuck With The Gas Pressure On The Control Of Nose Bleeding In Patients Presenting To The Emergency Department With Complaints Of Epistaxis

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201201078640N1

Enrollment

Registered

2016-03-13

Start date

2016-01-21

Completion date

Unknown

Last updated

2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epistaxis. Haemorrhage from nose Nosebleed

Interventions

Intervention 1: In the intervention group, we put the nose stuck on the patient's nose and after 15 min evaluate epistaxis scale compared to the initial state. Intervention 2: In the control group, pa

Treatment - Other

In the intervention group, we put the nose stuck on the patient's nose and after 15 min evaluate epistaxis scale compared to the initial state.

In the control group, patient wanted to hold his/her nose tightly and after 15 min evaluate epistaxis scale compared to the initial state.

Eligibility

Sex/Gender

All

Age

16 Years to 100 Years

Inclusion criteria

Inclusion criteria: 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.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Resolve Bleeding. Timepoint: 15 minutes later. Method of measurement: Direct Inspection.	—

Secondary

Measure	Time frame
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.	—

Measure

Time frame

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.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactHosein Amiri Largani

Shahid Sadoughi University of Medical Scienses

amirilargani@gmail.com+98 35 3626 8111

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026