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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04864613
Other study ID # 2636
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2019
Est. completion date December 30, 2020

Study information

Verified date April 2021
Source Ankara City Hospital Bilkent
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

In our study, we aim to predict palliative care patients earlier, to reduce hospitalization periods and to prevent intensive care unit occupation by palliative care patients.


Recruitment information / eligibility

Status Completed
Enrollment 135
Est. completion date December 30, 2020
Est. primary completion date July 8, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients older than 18 years will be included in the study. Patients staying longer than 48 hours intensive care will be included in the study. Exclusion Criteria: - Patients younger than 18 years. Patients staying less than 48 hours

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Ministry of Health Ankara City Hospital Ankara

Sponsors (1)

Lead Sponsor Collaborator
Ankara City Hospital Bilkent

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recognition of palliative care unit patients before intensive care discharge ENDING-S Scoring system used to predict patients who were followed up in intensive care units and discharged to palliative care unit during their hospitalization. We aim to identify patients who are likely to be admitted to palliative care centers following their admission to intensive care units, and to prepare a palliative care center before the discharge from the intensive care. Fourth day of intensive care follow up
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