- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01250626
Establish the Caring Model of Children With Chronic Kidney Disease and End-stage Renal Disease: To Set up Childhood Glomerular Filtration Rate (GFR) Formula in Taiwan
November 30, 2010 updated by: China Medical University Hospital
Inulin's usefulness as a diagnostic agent is based on the method of its elimination from the body.
Inulin is biologically inert, unbound by plasma proteins, freely filtered at the glomerulus, and is neither reabsorbed, metabolized nor secreted by the kidneys.
It is excreted almost entirely by glomerular filtration.
Inulin clearance is considered to be identical to glomerular filtration rate (GFR).
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Actual)
80
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
No older than 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Pediatric OPD, age < 18 y/o.
Description
- Main inclusion criteria: Pediatric OPD, age < 18 y/o.
- Main exclusion criteria: Acute renal failure, edema, muscular dystrophy, pleural effusion, ascites, malnutrition, neurogenic bladder, heart failure and ketoacidosis. And taken cimetidine or trimethoprim, and accepted renal replacement therapy.
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
- Observational Models: Case-Only
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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a single-group study
Pediatric OPD, age < 18 y/o.
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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
August 1, 2010
Study Registration Dates
First Submitted
November 29, 2010
First Submitted That Met QC Criteria
November 30, 2010
First Posted (Estimate)
December 1, 2010
Study Record Updates
Last Update Posted (Estimate)
December 1, 2010
Last Update Submitted That Met QC Criteria
November 30, 2010
Last Verified
August 1, 2010
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- DMR99-IRB-139
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.