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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01092260
Other study ID # 2009/741
Secondary ID
Status Completed
Phase N/A
First received March 23, 2010
Last updated January 3, 2012
Start date April 2010
Est. completion date December 2011

Study information

Verified date January 2012
Source Haukeland University Hospital
Contact n/a
Is FDA regulated No
Health authority Norway:National Committee for Medical and Health Research Ethics
Study type Observational

Clinical Trial Summary

The purpose of this study is to validate a feasible, safe and reliable iohexol plasma clearance method in routine monitoring of the renal function (GFR) in children.

Different parameters of renal function will be compared to the gold standard multiple sample points procedure of iohexol clearance.


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group N/A to 17 Years
Eligibility Inclusion Criteria:

- Age < 18 years

- Clinical indication for measurement of glomerular filtration rate

Exclusion Criteria:

- Previous serious reaction on Iohexol

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Norway Haukeland University Hospital Bergen

Sponsors (2)

Lead Sponsor Collaborator
Haukeland University Hospital Oslo University Hospital

Country where clinical trial is conducted

Norway, 

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