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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02653885
Other study ID # YIH
Secondary ID
Status Completed
Phase N/A
First received January 11, 2016
Last updated January 12, 2016
Start date January 2011
Est. completion date December 2014

Study information

Verified date January 2016
Source Ankara University
Contact n/a
Is FDA regulated No
Health authority Turkey: Ethics Committee
Study type Observational

Clinical Trial Summary

The outcome predictors for cardiac surgery has been popular for many researchers and clinicians. Determining risk factors before surgery reduce morbidity and mortality after surgery. Some routine blood results have been used as predictors for cardiac surgery but none of the researches studied red cell distribution width, mean platelet volume, platelet/lymphocyte ratio and neutrophil/lymphocyte ratio. This study focused on these parameters and to see whether these parameters can be predictors for cardiac surgery.


Recruitment information / eligibility

Status Completed
Enrollment 1500
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- elective, on-pump cardiac surgery

Exclusion Criteria:

- emergent cases

- pediatric cases

- congenital surgery

- heart transplantation

Study Design

Observational Model: Case-Crossover, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Other:
Red red cell distribution width
Results from hemogram

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ankara University

Outcome

Type Measure Description Time frame Safety issue
Primary incidence of combined adverse effects 48 hours Yes
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