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Effect of Traumastem powder use in control of nose bleeding

Comparison the Effect of Traumastem powder with a routine tampon in the treatment of non-traumatic epistaxis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130224012592N6
Enrollment
200
Registered
2018-10-08
Start date
2018-10-23
Completion date
Unknown
Last updated
2018-11-05

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: Intervention group 1: In this group, a thin layer of Traumastem powder (powder -2 gram-company BIOSTER, A.S - Veverská Bítýška- Czech Republic) onto a nose will be applied area by repe

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: All non traumatic epistaxis 18-65 years old patients Patients with normal blood pressure

Exclusion criteria

Exclusion criteria: Coagulopathy (INR>1.5) Multiple trauma Nasal trauma patients with shock not willing to participate in the research

Design outcomes

Primary

MeasureTime frame
Time of bleeding control. Timepoint: The time between tampon inserted and bleeding control. Method of measurement: With stopwatch.;Patient satisfaction. Timepoint: After the end of treatment, we will ask from patient about satisfaction of treatment. Method of measurement: Visual Analog Scale. This scale contains 1-10 scores that score 1 shows dissatisfaction and score 10 show excellent satisfaction.

Secondary

MeasureTime frame
Recurrence of bleeding in 24 hours. Timepoint: Calling to patients or his/her family. Method of measurement: With phone.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarzad Rahmani

Tabriz University of Medical Sciences

farzadrhn88@gmail.com+98 41 3549 8144

Outcome results

None listed

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