- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03262883
The Prevalence of Chronic Critical Illness in Turkey
The Prevalence of Chronic Critical Illness Adult Intensive Care Units in Turkey
Study Overview
Status
Conditions
Detailed Description
The patients who survive an acute critical illness in the Intensive Care Unit (ICU) may be delayed in a situation where they are sometimes totally independent before hand due to iatrogenic causes such as infections, dysfunctions, psychological disorders. This can take weeks, sometimes months. This disease is called "Chronic Critical Illness" (CCI).
Most researchers associate CCI with the need for prolonged acute mechanical ventilation or the opening of tracheostomy for prolonged acute mechanical ventilation. There is no single condition that does not require an extended mechanical ventilation from CCI. In conclusion, CCI is characterized by long-term care requiring survival and it is predicted that the cost of these patients will increase with the new patients whose cost will be added in the coming years. In the United States, the number of CCI is around 250,000, and this figure has increased by 50-100% in the last 10 years. At least 50% of these patients die in one year and less than 12% recover and become discharged. The annual cost of these patients' health care system is over $ 20 billion. The prevalence of CCI in Turkey is still unknown. In this study, it was aimed to investigate the prevalence of patients with Chronic Critical Syndrome in intensive care units in Turkey.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Van, Turkey, 65080
- Yuzuncu Yıl University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
The patient who is over 18 years old, taking mechanical ventilation support and staying in the critical care unit at least 8 days. Additional criterias; Clinical diagnosis of following situations:
- Prolonged mechanical ventilation
- Tracheotomia
- Sepsis
- Serious injury (burn)
- Stroke ( hemorhagic or ischemic)
- Traumatic brain injury
Exclusion Criteria:
- The patients who not having mechanical ventilation support
- The patient staying less than 8 days in the intensive care unit
- The patient younger than 18 years old
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Chronic Critical Illness
The patients who is over 18 years old and staying in the critical care unit at least 8 days. Additional criterias:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Critical care unit mortality
Time Frame: 30 day and 90 day
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The mortality change rates in the 30th days and 90th days
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30 day and 90 day
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Critical care unit costs
Time Frame: Duration of intensive care unit stay (8 day after the hospitalisation to sixth month)
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Costs of patients staying in the intensive care unit
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Duration of intensive care unit stay (8 day after the hospitalisation to sixth month)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hilmi Demirkıran, Official of the university
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Chronic critical illness
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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