Synechie Afrer Rhinosug. Proc. 2024

June 26, 2024 updated by: Mateusz Jan Stępiński

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

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.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

243

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Poland
    • Woj. Lubuskie
      • Gorzów Wielkopolski, Woj. Lubuskie, Poland, 66-400
        • Multidisciplinary Regional Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

Patients who were operated in Polish hospital (Gorzów Wlkp).

Description

Inclusion Criteria:

  • septo or septoconchoplasty

Exclusion Criteria:

  • incompleted documentation

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Control group
Patients underwent septoconchoplasty with or without turbionplasty. Surgeons didn't use nasal splits.
Other: Cottle's septoplasty and radiocoagulation conchoplasty
Cottle's septoplasty and radiocoagulation conchoplasty Study group - added nasal splits; Control group - nasal splits weren't used.
Study group
Patients underwent septoconchoplasty with or without turbionplasty. Surgeons used nasal splits.
Other: Cottle's septoplasty and radiocoagulation conchoplasty
Cottle's septoplasty and radiocoagulation conchoplasty Study group - added nasal splits; Control group - nasal splits weren't used.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Synechie
Time Frame: Between 2 weeks to 12 month
Intranasal synechiae after rhino nasal procedures
Between 2 weeks to 12 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Mateusz Jan Stępiński

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 26, 2024

Primary Completion (Actual)

June 26, 2024

Study Completion (Actual)

June 26, 2024

Study Registration Dates

First Submitted

June 26, 2024

First Submitted That Met QC Criteria

June 26, 2024

First Posted (Actual)

July 1, 2024

Study Record Updates

Last Update Posted (Actual)

July 1, 2024

Last Update Submitted That Met QC Criteria

June 26, 2024

Last Verified

June 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • SYNECHIE2024

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

Publication of results in open access magazine

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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