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Study identifier: NCT07531810 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Patient-Reported Outcomes and Complications After Structural Rhinoplasty Using Septal Extension Grafts

Condition: Nasal Deformity · Rhinoplasty · Nasal Obstruction  ·  Sponsor: Cumhuriyet University Hospital

PhaseN/A
Planned participants50
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Structural rhinoplasty with septal extension graft (SEG) is commonly used to achieve stable nasal tip support and predictable long-term outcomes. However, surgical success is not limited to structural stability alone and should also be evaluated from the patient's perspective. Patient-reported outcome measures (PROMs) have gained increasing importance in rhinoplasty, as they reflect patient satisfaction and perceived nasal function. Despite the widespread use of SEG, prospective studies evaluating PROMs together with postoperative clinical findings over time remain limited. This prospective observational cohort study aims to evaluate longitudinal changes in patient-reported outcomes and postoperative findings in adult patients undergoing primary structural rhinoplasty with SEG-based nasal tip support. Validated PROM instruments will be applied preoperatively and during routine postoperative follow-up visits at approximately 1, 3, and 6 months. In addition, postoperative complications and revision procedures will be recorded. The study aims to provide a more comprehensive understanding of patient-centered outcomes and their relationship with clinical findings in SEG-based rhinoplasty.

This description comes directly from the study's public registry record.

Talk to the study team

Murat Çelik, Assistant Professor  ·  +905546902104  ·  mucetr@gmail.com

Handan Derebaşınlıoğlu, Associate Professor  ·  +905322408767  ·  handanderebasinlioglu@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Sivas Cumhuriyet UniversitySivas, Sivas, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07531810