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NCT01323413 Clinical Trial

Determinants of Penumbra in Acute Ischemic Stroke Patients

Acute Ischemic Stroke Clinical Trial

Official title:
Determinants of Penumbra in Acute Ischemic Stroke Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01323413
Other study ID # 0080-11CTIL
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 2011
Est. completion date December 2016

Study information
Verified date June 2020
Source Rambam Health Care Campus
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of the study is to examine the influence of demographic, clinical and laboratory characteristics on the presence and size of penumbra in acute ischemic stroke patients and to determine those of them which related significantly and independently to the presence and size of Penumbra. The examined factors will include demographic variables such as age, gender, ethnic background, vascular risk factors and medical history, clinical parameters such as time from stroke onset until arrival to the hospital, results of neurological evaluation by NIHSS and imaging findings, laboratory tests such as body temperature, blood pressure, glucose level, renal functions etc. and imaging findings - the presence and the size of collateral blood vessels, the state of carotid arteries (by CTA). The possible correlation between all this parameters and the presence and the size of penumbra as detected by CTP will be further examined.

Recruitment information / eligibility
Status Completed
Enrollment 250
Est. completion date December 2016
Est. primary completion date November 2016
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Acute ischemic stroke patients hospitalized in Rambam Health Care Campus between 2008-2010, and which have underwent neurological evaluation including NIHSS scale, Brain CT, CT angio and Ct perfusion.

Exclusion Criteria:

- Intracranial hemorrhage of any other brain condition

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Israel Rambam Health Care Campus Haifa

Sponsors (1)
Lead Sponsor Collaborator
Rambam Health Care Campus

Country where clinical trial is conducted

Israel, 

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