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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02917811
Other study ID # 20042016
Secondary ID
Status Completed
Phase N/A
First received September 13, 2016
Last updated March 29, 2017
Start date January 2016
Est. completion date November 2016

Study information

Verified date March 2017
Source Università degli Studi di Ferrara
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to verify if high values of RDW are useful prognostic marker for ICU mortality and 90-days mortality. Moreover, we will investigate the prognostic value of RDW in specific subgroup population with some clinical characteristic wich may modify RDW baseline values, i.e. transfused patients or patients with high markers of hemolysis


Recruitment information / eligibility

Status Completed
Enrollment 250
Est. completion date November 2016
Est. primary completion date October 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Unselected ICU patients

Exclusion Criteria:

- Length of stay in ICU <48 hours

- Hematological disease

- Age <18 years

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Italy Sant'Anna Hospital Ferrara

Sponsors (1)

Lead Sponsor Collaborator
Università degli Studi di Ferrara

Country where clinical trial is conducted

Italy, 

References & Publications (2)

Kim CH, Park JT, Kim EJ, Han JH, Han JS, Choi JY, Han SH, Yoo TH, Kim YS, Kang SW, Oh HJ. An increase in red blood cell distribution width from baseline predicts mortality in patients with severe sepsis or septic shock. Crit Care. 2013 Dec 9;17(6):R282. d — View Citation

Lorente L, Martín MM, Abreu-González P, Solé-Violán J, Ferreres J, Labarta L, Díaz C, González O, García D, Jiménez A, Borreguero-León JM. Red blood cell distribution width during the first week is associated with severity and mortality in septic patients — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary 90-days mortality 90 days
Secondary ICU mortality 90 days
Secondary Length of mechanical ventilation 90 days
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