Ireland
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Recruiting Not applicable

Lateral Crural Steal With Columellar Strut Graft in Primary Open Rhinoplasty

NCT07317947 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-01-05
Last updated
2026-01-09

Condition(s) studied

RhinoplastyNasal SurgeryAesthetic Outcomes

Investigational drug(s) / intervention(s)

Lateral crural steal with columellar strut graft in Primary Open Rhinoplasty

Lateral crural steal with columellar strut graft in Primary Open Rhinoplasty: Patients undergo primary open rhinoplasty under general anesthesia. After local infiltration, an open approach is performed using an inverted-V transcolumellar incision with bilateral marginal incisions. The skin-soft tissue envelope is elevated in the supra-perichondrial plane. Dorsal deformities are corrected and septoplasty is performed with cartilage harvest. Vestibular skin is undermined and cephalic trimming of the lateral crura is carried out. Lateral crural steal is performed by advancing the medial end of the lateral crus 3-5 mm medially using transdomal sutures after defining the new dome position. A fixed columellar strut graft is inserted between the medial crura and secured to provide central tip support. Interdomal sutures are placed. No additional projection-enhancing grafts are used. Incisions are closed and internal and external nasal splints are applied.

Study summary

The goal of this clinical trial is to assess the effect of Lateral crural steal with Columellar strut graft done in Primary Open Rhinoplasty and its long-term sustainability on nasal tip projection and nasal tip rotation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: * Patients seeking primary rhinoplasty for aesthetic and/or functional indications. * Presence of inadequate nasal tip projection and/or rotation suitable for correction using lateral crural steal with columellar strut graft. * Ability to provide written informed consent and comply with follow-up visits. Exclusion Criteria: * History of prior nasal surgery. * History of severe nasal trauma, altering cartilage architecture. * Significant functional nasal obstruction requiring complex external nasal valve reconstruction. * Patients with excessively wide alar base requiring alar base reduction involving vestibular sill excision (to prevent confounding on projection/rotation). * Patients with facial skeletal or developmental abnormalities e.g. maxillary hypoplasia, maxillary prognathism, dentofacial deformities. * Patients with psychiatric illness or Body Dysmorphic Disorder. * Significant medical comorbidities contraindicating elective surgery or general anesthesia. * Inability to provide informed consent or comply with follow-up.

Primary outcome measure(s)

  • Nasal tip projection. — Analysis will be done preoperatively, immediate postoperatively, and at 6-month and 1-year postoperatively.
    Assessing nasal projection using Goode's ratio, which is the ratio between distance from the alar crease (vertical plane of the alar base) to the tip of the nose and distance from the nasion to the tip of the nose. The ideal ratio is between 0.55 to 0.60. Nasal tip projection will be assessed using Rhinobase® software developed by Apaydin et al (2009), which is a software for rhinoplasty that enables standardized photographic analysis, facilitates precise anthropometric measurements, and provides objective documentation of pre- and postoperative nasal parameters.
  • Nasal tip rotation — Analysis will be done preoperatively, immediate postoperatively, and at 6-month and 1-year postoperatively.
    Assessing nasal tip rotation through measuring the Nasolabial angle which is the angle formed at the junction of the columella and a line drawn from the subnasale to the labrale superius, and the Nasofacial angle which is the angle between the nasal dorsum and the facial plane (glabella to pogonion). Nasal tip rotation will be assessed using Rhinobase® software developed by Apaydin et al (2009), which is a software for rhinoplasty that enables standardized photographic analysis, facilitates precise anthropometric measurements, and provides objective documentation of pre- and postoperative nasal parameters.

Trial sites (1)

FacilityCityRegionStatus
Kafrelsheikh University Hospital Kafr ash Shaykh Egypt Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07317947 on ClinicalTrials.gov ↗ ← All trials in Egypt