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Investingation on Outcomes After Combining Septoplasty With Additional Procedures.

NCT07127848 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2025-08-17

No results posted yet for this study

Summary

The aim of this study will be to compare postoperative nasal airflow and symptom improvement using a NOSE form in patients after different types of surgical treatment. Patients will be treated with one of the following operations: septoplasty with turbinectomy, septoplasty with radiofrequent ablation of the nasal turbinates, or septoplasty with valvuloplasty.

This is a single-center prospective randomized interventional comparative study on patients in a tertiary rhinology center, who will undergo septoplasty alongside one additional rhinologic procedure aimed at improving nasal patency.

Conditions

  • Nasal Patency
  • Breathing Disorder During Sleeping
  • Breathing Mechanics

Interventions

PROCEDURE

Septoplasty with Mucotomy

Subtotal reconstruction of the nasal septum accompanied by radiofrequent nasal mucosal reduction of the inferior turbinates.

PROCEDURE

Septoplasty with Turbinectomy

Subtotal reconstruction of the nasal septum accompanied by surgical resection of the inferior turbinates.

PROCEDURE

Septoplasty with Valvuloplasty

Subtotal reconstruction of the nasal septum accompanied by surgical intervention by placing a flare sutture in the internal nasal valve area.

Sponsors & Collaborators

  • University Hospital Sestre Milosrdnice

    lead OTHER

Principal Investigators

  • Andro Košec, MD, PhD, FEBORL-HNS, FACS · University Hospital Center Sestre milosrdnice, Department of ORL&HNS

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-04-01
Primary Completion
2025-09-03
Completion
2025-09-03

Countries

  • Croatia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07127848 on ClinicalTrials.gov