Association Between Urine Concentration Ability and the Progression of Chronic Kidney Disease

August 24, 2011 updated by: Benaya Rozen-Zvi

The study hypothesis is that urine concentrating ability can predict the rate of kidney function decline.

Patients with kidney disease at the investigatorsclinic will be asked to give first morning urine sample and osmolarity will be measured. The investigators will follow up kidney function decline and check if there is association with urine osmolarity.

Study Overview

Status

Unknown

Detailed Description

Design:

Prospective observational study

Setting:

Predialysis clinic.

Participants:

We will include adults >18 years providing signed informed consent.

Inclusion:

Patients with CKD and estimated GFR of less then 50 mL per minute estimated by the short MDRD equation base on two creatinine values taken at least two weeks apart and are not getting steroids or immunosuppressive medication as treatment for their primary kidney disease.

Exclusion:

  1. Life expectancy of less then 6 month.
  2. Expected to start renal replacement therapy within 3 month.
  3. Acute or acute on chronic renal failure with reversible component.
  4. Treatment with AVP inhibitors.
  5. Chronic hyponatremia (Na+<135 in two measurement two weeks apart).
  6. Primary polydipsia.
  7. Inability to give informed consent.
  8. Clinical hypovolemia.

Outcomes:

Primary outcomes:

Rate of GFR decline as assessed by short MDRD equation with at least three measurements at least three month apart.

. Secondary efficacy

  1. Rate of ESKD define as need RRT.
  2. Overall mortality.
  3. ESKD and overall mortality.
  4. Blood pressure as assessed by clinic measurement.
  5. Protein creatinine ratio in random urine sample.
  6. Hemoglobin level.
  7. Need for erythropoietin treatment.
  8. Blood level of 25OH vitamin D and 1,25OH vitamin D.
  9. PTH, calcium and phosphate level.
  10. The occurrence of edema by physical evaluation.

Predefined subgroup analysis:

  1. Diabetic patients.
  2. Patients treated with diuretics.

Sample size:

We will need to recruit about 200 patients.

Statistical methods:

We will use linear regression analysis with 95% CI for the continuous variable. And chi square for dichotomous variable.

Data collection and trial flow:

All patients in predialysis clinic of Dan district of "Kupat holim clalit" will be screen. Patients fulfilling inclusion criteria will be approached by trial investigator for informed consent and trial recruitment. For patients fulfilling inclusion criteria that will not consent to participate we will be record name and ID without further details. Consenting patients will bring the three samples of first voided urine of the morning for osmolarity, PH, sodium, potassium and chloride.

Patient recruitment:

Baseline data collection:

Collection of data will include baseline conditions, primary kidney disease, current medications, clinical evaluation for edema and blood pressure.

Laboratory results will include creatinine, urea, sodium, potassium, GFR assessed by short MDRD equation, protein creatinine ratio in random urine sample Hb level, vitamin D level calcium, phosphorus and PTH.

Follow-up and outcome data collection:

  1. Creatinine, estimated GFR, urea, sodium, potassium chloride, hemoglobin and protein creatinine ratio in random urine sample at least every three month
  2. Clinical assessment for edema and blood pressure ant least every three month.
  3. Time to initiation of dialysis or transplantation.
  4. Mortality of any cause and cardiovascular mortality.
  5. Hospitalization for any cause and the length of hospital stay.
  6. The need for ESA treatment and ESA dose will be recorded.

Study Type

Observational

Enrollment (Anticipated)

200

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

      • Ganey Tiqua, Israel, 55900
        • Pre dialysis clinic Dan Petach Tiqua county General health service
        • Contact:
        • Contact:

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

Patients with CKD and estimated GFR of less then 50 mL per minute.

Description

Inclusion Criteria:

  • Patients with CKD and estimated GFR of less then 50 mL per minute estimated by the short MDRD equation base on two creatinine values taken at least two weeks apart and are not getting steroids or immunosuppressive medication as treatment for their primary kidney disease.

Exclusion Criteria:

  1. Life expectancy of less then 6 month.
  2. Expected to start renal replacement therapy within 3 month.
  3. Acute or acute on chronic renal failure with reversible component.
  4. Treatment with AVP inhibitors.
  5. Chronic hyponatremia (Na+<135 in two measurement two weeks apart).
  6. Primary polydipsia.
  7. Inability to give informed consent.
  8. Clinical hypovolemia.

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
Measure Description
Time Frame
eGFR slope
Time Frame: 12 month
Creatinnie value will be measured at least every three month and eGFR will be calculated by MDRD equation. A regression line will be plotted against time and the eGFR slope will be calculated.
12 month

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Benaya Rozen-Zvi, MD, General health services - Dan Petach tiqua county

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

October 1, 2011

Primary Completion (Anticipated)

October 1, 2013

Study Completion (Anticipated)

October 1, 2013

Study Registration Dates

First Submitted

August 23, 2011

First Submitted That Met QC Criteria

August 24, 2011

First Posted (Estimate)

August 25, 2011

Study Record Updates

Last Update Posted (Estimate)

August 25, 2011

Last Update Submitted That Met QC Criteria

August 24, 2011

Last Verified

August 1, 2011

More Information

Terms related to this study

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.

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