Consistency Between Measures of Renal Function in ICU Patients

May 19, 2022 updated by: Johan Petersson, Karolinska University Hospital
This study aim to compare different measures of renal function (glomerular filtration rate) in ICU patients.

Study Overview

Detailed Description

The study uses a large dataset of prospectively collected data according to clinical routines.

Study Type

Observational

Enrollment (Anticipated)

5000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Stockholm, Sweden, 17176
        • Karolinska University Hospital Solna

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

General ICU patients

Description

Inclusion Criteria:

  • ICU patients with at least one measurement of urinary creatinine clearance

Exclusion Criteria:

  • Renal replacement therapy initiated before the measurement of creatinine clerance

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Correlations between estimates of renal function
Time Frame: 7 days
7 days
Correlations between changes in estimates of renal function
Time Frame: 7 days
7 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 1, 2006

Primary Completion (ACTUAL)

December 31, 2017

Study Completion (ANTICIPATED)

December 31, 2024

Study Registration Dates

First Submitted

December 12, 2021

First Submitted That Met QC Criteria

May 19, 2022

First Posted (ACTUAL)

May 23, 2022

Study Record Updates

Last Update Posted (ACTUAL)

May 23, 2022

Last Update Submitted That Met QC Criteria

May 19, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

No plan.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Critical Illness

Clinical Trials on S Creatinine concentration

Subscribe