Synechie Afrer Rhinosug. Proc. 2024
Completed
- Conditions
- Complication of Surgical Procedure
- Registration Number
- NCT06482866
- Lead Sponsor
- Mateusz Jan Stępiński
- Brief Summary
Analyze the factors influencing the development of intranasal adhesions (synechiae), with particular emphasis on the use of nasal septal separators, and to suggest a solution to reduce this complication in the future.
Analyze of the medical documentation. It was not an experimental examination.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 243
Inclusion Criteria
- septo or septoconchoplasty
Exclusion Criteria
- incompleted documentation
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Synechie Between 2 weeks to 12 month Intranasal synechiae after rhino nasal procedures
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms contribute to intranasal synechiae formation after endonasal surgery?
How effective are nasal septal separators compared to standard-of-care treatments in preventing post-surgical adhesions?
Are there specific biomarkers that identify patients at higher risk for developing intranasal synechiae following Cottle's septoplasty?
What adverse events are commonly associated with radiocoagulation conchoplasty in endonasal surgical procedures?
What combination therapies or alternative interventions show promise in reducing intranasal adhesion complications compared to nasal septal separators?
Trial Locations
- Locations (1)
Multidisciplinary Regional Hospital
🇵🇱Gorzów Wielkopolski, Woj. Lubuskie, Poland
Multidisciplinary Regional Hospital🇵🇱Gorzów Wielkopolski, Woj. Lubuskie, Poland