Clinical trial Recruiting at 1 site Observational Ages 18 and up

Patient-reported outcomes and complications after structural rhinoplasty with septal extension grafts

Official title: Patient-Reported Outcomes and Complications Following Structural Rhinoplasty Using Septal Extension Grafts: A Prospective Cohort Study

Run by Cumhuriyet University Hospital · NCT07531810 · Data updated 2026-11-12

This project will track adults having their first structural rhinoplasty with a septal extension graft to see how their symptoms, satisfaction, and any complications change over the first six months after surgery.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment50 (estimated)
SponsorCumhuriyet University Hospital
Academic / other
Locations1 site (Sivas, Sivas)
StatusRecruiting
StartedApril 1, 2026
Main results expectedMarch 2027
Study endsJune 2027
Registry record updatedJune 22, 2026
Trial IDNCT07531810 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 and older planning a primary structural rhinoplasty with a septal extension graft who can complete questionnaires and attend follow-up visits are ideal candidates.

Probably not a fit

Patients undergoing revision rhinoplasty, concurrent major craniofacial procedures, or those unable to complete preoperative PROMs or attend follow-ups are unlikely to benefit from the study's findings.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This single-center prospective observational cohort will enroll consecutive adults undergoing primary structural rhinoplasty with septal extension grafts, all performed by the same surgical team using a standardized structural approach. Validated patient-reported outcome measures (PROMs) and clinical findings will be collected preoperatively and at approximately 1, 3, and 6 months after surgery. The study will document postoperative complications and clinical signs such as tip stiffness, palpable grafts, columellar deviation, and the need for revision surgery. Investigators will correlate changes in PROM scores with clinical findings to better define patient-centered outcomes after SEG-based tip support.

Why it matters

Potential benefit: If successful, the results could help surgeons choose techniques that improve patient satisfaction and reduce complications after structural rhinoplasty with septal extension grafts.

How similar studies have gone: PROMs have been increasingly used in rhinoplasty and smaller or retrospective reports exist, but prospective longitudinal data specifically focused on septal extension grafts are limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 18 years or older
* Undergoing primary structural rhinoplasty with septal extension graft
* Able to understand and complete patient-reported outcome questionnaires (PROMs)
* Willing to participate and provide written informed consent

Exclusion Criteria:

* History of previous nasal surgery (revision rhinoplasty)
* Undergoing concomitant major craniofacial procedures
* Missing preoperative PROM data
* Unable to complete postoperative follow-up assessments

Where it's running

  • Sivas Cumhuriyet University
    Sivas, Sivas, Turkey (Türkiye)
    Recruiting

Study contacts

  • Principal investigator: Murat Çelik, Assistant Professor — Cumhuriyet University
  • Study coordinator: Murat Çelik, Assistant Professor
  • Email: mucetr@gmail.com
  • Phone: +905546902104

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.