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OpenTrials
Completed

NCT Number: NCT06482866

Synechie Afrer Rhinosug. Proc. 2024

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.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Multidisciplinary Regional Hospital

Gorzów Wielkopolski, Woj. Lubuskie, 66-400, Poland

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • septo or septoconchoplasty

Exclusion criteria

  • incompleted documentation

Treatment and study plan

Cottle's septoplasty and radiocoagulation conchoplasty

Other

Cottle's septoplasty and radiocoagulation conchoplasty Study group - added nasal splits; Control group - nasal splits weren't used.

Primary outcomes

  1. Synechie

    Time frame: Between 2 weeks to 12 month

    Intranasal synechiae after rhino nasal procedures

Sponsors and collaborators

Lead sponsor

Mateusz Jan Stępiński

Other

Registry information

Official study title

Risk Factors Leading to the Formation of Intranasal Synechiae in Patients After Endonasal Surgery

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Jul 1, 2024
Registry last updated
Jul 1, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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