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Renal Function Measurements in Children

NCT01092260 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 96

Last updated 2012-01-05

No results posted yet for this study

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.

Conditions

  • Renal Function Disorder

Sponsors & Collaborators

  • Oslo University Hospital

    collaborator OTHER

  • Haukeland University Hospital

    lead OTHER

Principal Investigators

  • Camilla Tondel, MD · Haukeland University Hospital, Bergen, Norway

Eligibility

Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-04-30
Primary Completion
2011-12-31
Completion
2011-12-31

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01092260 on ClinicalTrials.gov