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Recruiting NCT06805214

Increased Body Temperature Post Tracheostomy: a Retrospective Study

Observational Tracheostomy Complication

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: post tracheostomy fever.
Who it may be relevant to
Registry conditions: Tracheostomy Complication. Basic parameters: 18 years — 99 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Israel
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Tracheostomy is one of the most common procedures in intensive care units. Post-tracheostomy increased body temperature within 24 hours is common. However, frequently sepsis workup is performed along with initiation of broad spectrum antibiotic therapy. We will investigate the incidence of post tracheostomy fever and whether retrospectively the increased temperature indicated development of sepsis or not. The study is retrospective and will be based on data collection.

Interventions

  • Other post tracheostomy fever
    incidence of post tracheostomy fever and whether retrospectively the increased temperature indicated development of sepsis or not (no intervention)

Primary outcome measures

  • Post tracheostomy fever [Time frame: 24 hours post tracheostomy]

Eligibility criteria

Inclusion Criteria: Patients admitted to the ICU from 1.2020 to 1.2025 who underwent tracheostomy during ICU admission -

Exclusion Criteria: Patients who did not fullfil the above criteria

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Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Israel · 1 center
  • Meir Medical Center — Kfar Saba

Identifiers

NCT: NCT06805214 · 0021-25-MMC

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗