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NCT00117390 Clinical Trial

Evaluation of the Optimal Technique for Determination of Renal Function of Critically Ill Patients

Critical Illness Clinical Trial

Official title:
Evaluation of the Optimal Technique for Determination of the Renal Function of Critically Ill Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00117390
Other study ID # 2004/101
Secondary ID
Status Completed
Phase N/A
First received June 30, 2005
Last updated December 19, 2007
Start date June 2004
Est. completion date October 2006

Study information
Verified date December 2007
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority Belgium: Federal Agency for Medicines and Health Products, FAMHP
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the optimal technique for determination of the renal function of critically ill patients.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date October 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Over 18 years old

- Intensive care patient

- Given informed consent

- Arterial infusion

- A bladder catheter

Exclusion Criteria:

- Diurese < 400 mL/d

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Intervention

Procedure:
• Measurement of inulin clearance

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 Comparison of the determination of the renal function by other means than the golden standard, inulin clearance
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