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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00117416
Other study ID # 2002/382
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date February 2003
Est. completion date February 2003

Study information

Verified date July 2021
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the renal perfusion depending on the MAP.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date February 2003
Est. primary completion date February 2003
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Over 18 years old - Intensive care patient - Treated with vasopressor - Given informed consent - Arterial infusion - A bladder catheter Exclusion Criteria: - Anamneses of hypertension - Neurological trauma - Acute renal insufficiency other than prerenal or acute tubular necrosis etiology - Hepatorenal syndrome - Treated with diuretics - Mechanical ventilation and unstable

Study Design


Intervention

Procedure:
controlling the MAP


Locations

Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary creatinine clearance after 4 hours
Secondary resistance index
Secondary diuresis
Secondary urinary indices of renal function
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