Effect of using Alar Contour Graft in Improvement of Respiratory Problems and Patients’ Satisfaction after Rhinoplasty

Determining the Effect of Alar Contour Graft in Improvement of Respiratory Problems and Patients’ Satisfaction after Rhinoplasty Based on Vertical Dome Division

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2015062322889N1

Enrollment

211

Registered

2015-07-19

Start date

2013-10-23

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

patients scheduled for rhinoplastiy surgery. Deviated nasal septum

Interventions

Intervention 1: control group:rhinoplasty based onvertical dome division technique. Intervention 2: intervention group:rhinoplasty based onvertical dome division technique using alar contour graft.

Treatment - Surgery

control group:rhinoplasty based onvertical dome division technique

intervention group:rhinoplasty based onvertical dome division technique using alar contour graft

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: The patients candidate for rhinoplasty in 1393 in Khalili Hospital, Shiraz; Completing consent form; Completing demographic information and questionnaire Exclusion criteria: Patient’s with nasal polyp; Systemic disorders that postpones the wound healing; History of nasal trauma; Psychiatric disorders preventing an unbiased post-op evaluation; Poor follow up; Severe septal deviation diagnosed by P/E preoperatively; Congenital deformity; Using spreader graft with any causes

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Respiratory problem including airway obstruction. Timepoint: before the surgery, 1 month and 6 months after the surgery. Method of measurement: questionnaire and physical exam.	—

Secondary

Measure	Time frame
Patients' satisfaction from surgary. Timepoint: 1 month and 6 months after the surgery. Method of measurement: questionnaire and physical exam.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Saeid Pourseirafi

Shiraz University of Medical Sciences

dr.s.pourseirafi@gmail.com pourseirafi@sums.ac.ir+98 31 4524 8966

Outcome results

None listed

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