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The effect of spreader on the aesthetic and respiratory issues of rhinoplasty patients

Comparison between doing and not doing spreader(graft or flap) in rhinoplasty patients with hump more than 3mm with respect to aesthetic and respiratory issues

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201109049320N1
Enrollment
60
Registered
2020-12-12
Start date
2020-11-21
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Rhinoplasty patients with a hump greater than 3 mm. Other specified disorders of nose and nasal sinuses

Interventions

Intervention 1: Intervention group: Spreader (graft or flap) in rhinoplasty patients with a hump of more than 3 mm. Intervention 2: Control group: Do not do a spreader (graft or flap) in rhinoplasty p

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Absence of clinical problems for the patient Patient consent to participate in the study

Exclusion criteria

Exclusion criteria: Existence of structural problems such as: nasal obstruction and a history of deformity that requires rhinoplasty.

Design outcomes

Primary

MeasureTime frame
Nasal congestion. Timepoint: Before and after surgery. Method of measurement: Breathing quality score.

Secondary

MeasureTime frame
Severe deviation of the nasal septum. Timepoint: Before and after surgery. Method of measurement: clinical examination.;The presence or absence of shortness of breath. Timepoint: Before and after surgery. Method of measurement: Clinical examination.;Right nasal resistance. Timepoint: Before and after surgery. Method of measurement: Rhinoomanometry test by active anterior rhinomanometry according to the protocol of the International Committee for Standardization.;Left nasal resistance. Timepoint: Before and after surgery. Method of measurement: Rhinoomanometry test by active anterior rhinomanometry according to the protocol of the International Committee for Standardization.;Total resistance. Timepoint: Before and after surgery. Method of measurement: Rhinoomanometry test by active anterior rhinomanometry according to the protocol of the International Committee for Standardization.;Right nasal airflow. Timepoint: Before and after surgery. Method of measurement: Rhinoomanometry test by active anterior rhinomanometry according to the protocol of the International Committee for Standardization.;Left nasal airflow. Timepoint: Before and after surgery. Method of measurement: Rhinoomanometry test by active anterior rhinomanometry according to the protocol of the International Committee for Standardization.;Total air flow (units: Pascals per milliliter per second). Timepoint: Before and after surgery. Method of measurement: Rhinoomanometry test by active anterior rhinomanometry according to the protocol of the International Committee for Standardization.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRoozbeh Rahbar

Ahvaz University of Medical Sciences

rahbar-r@ajums.ac.ir061355402546

Outcome results

None listed

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