NCT06482866

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
243

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 26, 2024

Completed
Same day until next milestone

Study Start

First participant enrolled

June 26, 2024

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 26, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 26, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

July 1, 2024

Completed
Last Updated

July 1, 2024

Status Verified

June 1, 2024

Enrollment Period

Same day

First QC Date

June 26, 2024

Last Update Submit

June 26, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Synechie

    Intranasal synechiae after rhino nasal procedures

    Between 2 weeks to 12 month

Study Arms (2)

Control group

Patients underwent septoconchoplasty with or without turbionplasty. Surgeons didn't use nasal splits.

Other: Cottle's septoplasty and radiocoagulation conchoplasty

Study group

Patients underwent septoconchoplasty with or without turbionplasty. Surgeons used nasal splits.

Other: Cottle's septoplasty and radiocoagulation conchoplasty

Interventions

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

Control groupStudy group

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

  • septo or septoconchoplasty

You may not qualify if:

  • incompleted documentation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Multidisciplinary Regional Hospital

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

Location

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Lek.

Study Record Dates

First Submitted

June 26, 2024

First Posted

July 1, 2024

Study Start

June 26, 2024

Primary Completion

June 26, 2024

Study Completion

June 26, 2024

Last Updated

July 1, 2024

Record last verified: 2024-06

Locations