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The use of Neozoheam nasal gel in the epistaxis treatment : Convenience OR Discomfort

Comparison of Nosoheam nasal gel and anterior nasal tampon in epistaxis treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016121222181N2
Enrollment
100
Registered
2017-01-08
Start date
2016-04-20
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. Epistaxis

Interventions

Intervention 1: The trained physician entered Nozoheam gel tube into the patient’s nose about 1-1.5Cm and emptied the contents of tube with fast pressure while getting the nose with thumb and point fi
Treatment - Drugs
Treatment - Other
The trained physician entered Nozoheam gel tube into the patient’s nose about 1-1.5Cm and emptied the contents of tube with fast pressure while getting the nose with thumb and point fingers. In the ca
First, a cotton ball, previously socked in a mixture of 2% lidocaine and 1:100000 epinephrine, was placed in the anterior nostril and after bleeding control, the nose was packed with tetracycline-impr

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criterion: anterior nasal bleeding mild to moderate. Exclusion criteria: patients who were admitted with epistaxis under the age of 16 years old; posterior and severe bleeding nose; bleeding visible vessels; severe coagulation disorders or thrombocytopenia less than INR 50,000 or top 5 or hemophilia or patients treated with antibiotics anticoagulant; severe trauma to the nose and face; people in shock; and others excluded patients with anterior nasal bleeding were enrolled.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Satisfaction. Timepoint: During discharge. Method of measurement: Visual Analogous Scale.

Secondary

MeasureTime frame
Pain during procedure. Timepoint: After procedure. Method of measurement: Visual Analogous Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi Torabi

Kerman University of Medical Sciences

me_torabi@kmu.ac.ir+98 34 3223 5011

Outcome results

None listed

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