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Effect of osteotomy on satisfaction of patient with nasal bone fracture regarding nose appearance

Clinical trial of the comparison between closed reduction and closed reduction in conjunction with osteotomy on satisfaction of patients with acute nasal bone fracture

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016030926987N1
Enrollment
80
Registered
2016-04-08
Start date
2015-03-01
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

Nasal bone fracture. Fracture of nasal bones

Interventions

Intervention 1: Intervention group: Firstly, all patients underwent traditional closed reduction procedure. Then in the presence of post reduction deformity, internal osteotomy procedure was performed
Treatment - Surgery
Treatment - Drugs
Intervention group: Firstly, all patients underwent traditional closed reduction procedure. Then in the presence of post reduction deformity, internal osteotomy procedure was performed at the time of
Control: all patients only underwent traditional closed reduction procedure. Even in the presence of post reduction deformity, no further correcting procedure was performed.

Sponsors

Vice chancellor for research of Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criterion: acute nasal bone fracture during 7-10 days before intervention. Exclusion criteria: naso-orbitoethmoid (NOE) fractures; nasal bone fracture associated with any other fracture of facial bones; fractures lead to maxilla dropping; and multiple septal fractures.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Patients satisfaction with nose appearance. Timepoint: 4 months after intervention. Method of measurement: questionnaire.

Secondary

MeasureTime frame
Post reduction deformity. Timepoint: 4 months after intervention. Method of measurement: Surgeon evaluation by clinical examination.;Intervention's complications. Timepoint: 4 months after intervention. Method of measurement: Clinical examination by Surgeon.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZeinab Shajirat

Ahvaz Jundishapur University of Medical Sciences

Zeinab.shajirat@gmail.com+98 61 3221 6504

Outcome results

None listed

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