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Observational Prospective Study of the Predicted Value of Immature Thrombocytes Counts in Three Different Groups of Critically Ill Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02016859
Enrollment
500
Registered
2013-12-20
Start date
2014-01-31
Completion date
2014-11-30
Last updated
2013-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Critically Ill Patients, Neutropenic Fever Patients, Patients With Hip Fractures

Keywords

IPF Immature platelet fraction, ICU neutropenic fever, hip fracture, critically ill

Brief summary

Immature Platelet Fraction (IPF) is a new value in CBC blood tests Recent Studies showed that this value may be another prognostic factor in critically ill patients such as those admitted to ICU, or those with neutropenic Fever. The purpose of the study is to check if the IPF may be used as a prognostic Factor in these patients

Detailed description

In this study we have 3 groups of patients * Patients admitted to ICU * Patients admitted with neutropenic fever * Patients admitted with hip fractures it is a prospective study, not interventional, we'll take blood samples of these patients including CBC count eith IPF and other inflammation markers such as CRP and we'll compare CRP to IPF in addition to clinical follow-up of the patient till discharge. At the end of this study we'll compare the efficacy of IPF as a prognostic Factor in these patients

Interventions

OTHERImmature Platelet Fraction

Sponsors

Dr. Yishai Ofran
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

\- Admission to hospital blood sample is taken between 24:00 pm till 15:00 pm

Exclusion criteria

* blood sample is taken after 15:00 pm in the first day of admission during the week * blood sample is taken on weekend: thursday 15:00 pm till saturday 24:00 pm

Design outcomes

Primary

MeasureTime frameDescription
Time to recovery from sepsis or time to death6 monthsthe primary outcome is the result of the patient's admission on which data analysis will be based

Secondary

MeasureTime frameDescription
Predicting value of IPF for prognosisbaeline 6 monthsafter the analysis of the data we'll may ba able to assess the predicting value of the IPF in predicting severity of infection and prediciting prognosis of infection in the three groups described

Other

MeasureTime frameDescription
clinical use of IPF as a prognostic factorup to 12 monthsthis outcome is not uet based we need much more studies in order to be able to use IPF in daily clinical work

Countries

Israel

Contacts

Primary ContactYishai Ofran, Doctor
Y_ofran@ramabm.health.gov.il009720502061524
Backup ContactDoaa Okasha, doctor
d_okasha@rambam.health.gov.il009720502062701

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026