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The efficacy of diced cartilage and diced bone on correcting dorsum Deformities

Comparative study the efficacy of diced cartilage and diced bone on correcting dorsum deformities in rhinoplasty: randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250428065514N1
Enrollment
60
Registered
2025-06-08
Start date
2025-06-15
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Dorsum Deformities.

Interventions

Intervention 1: Intervention group (Diced bone group): During rhinoplasty surgery, diced bone will be prepared from the bone obtained from the hump (during humpectomy procedure) and from the bony spur

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 18 years old No sex restrictions Requiring rhinoplasty surgery to correct dorsal deformities Undergoing primary rhinoplasty with thin skin (defined as low skin thickness with Obagi grade 1), who exhibit bony dorsal irregularities at the time of surgery and after dorsal modifications. Signature of consent form

Exclusion criteria

Exclusion criteria: A history of cancer Cardiopulmonary disease, Hepatorenal dysfunction Costal cartilage with calcification Pregnant females or lactating females Individuals with autoimmune diseases, Recent local or systemic infection within the last month Those requiring revision rhinoplasty

Design outcomes

Primary

MeasureTime frame
Correcting dorsum deformities. Timepoint: 7 days, 1 &3 month after surgery. Method of measurement: Photograph.;Aesthetic Satisfaction Scale. Timepoint: 1 & 3 Month after surgery. Method of measurement: Based on visual analogue scale (VAS): Patients will indicate their satisfaction with the appearance of their nose on a 10-centimeter visual analogue scale (VAS).;The score on the Standardized Cosmesis and Health Nasal Outcome Survey (SCHNOS-C) questionnaire. Timepoint: 1 & 3 Month after surgery. Method of measurement: By Standardized Cosmesis and Health Nasal Outcome Survey(SCHNOS-C) questionnaire: This questionnaire consists of 10 items assessing nasal function and aesthetics.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Saeed Shirafkan

Ahvaz University of Medical Sciences

shirafkan-s@ajums.ac.ir+98 61 3311 0000

Outcome results

None listed

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