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

NCT ID: NCT00117390

Last Updated: 2007-12-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-06-30

Study Completion Date

2006-10-31

Brief Summary

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

Detailed Description

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Conditions

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Renal Function Critical Illness

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Interventions

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Measurement of inulin clearance

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Over 18 years old
* Intensive care patient
* Given informed consent
* Arterial infusion
* A bladder catheter

Exclusion Criteria

* Diurese \< 400 mL/d
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Ghent

OTHER

Sponsor Role lead

Principal Investigators

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Eric Hoste, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Ghent

Locations

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University Hospital Ghent

Ghent, , Belgium

Site Status

Countries

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Belgium

Related Links

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http://www.uzgent.be

Website of the University Hospital Ghent

Other Identifiers

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2004/101

Identifier Type: -

Identifier Source: org_study_id