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

Sponsor
Benaya Rozen-Zvi (Other)
Overall Status
Unknown status
CT.gov ID
NCT01423045
Collaborator
(none)
200
1
24
8.3

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase

    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 Design

    Study Type:
    Observational
    Anticipated Enrollment :
    200 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Association Between Urine Concentration Ability and the Progression of Chronic Kidney Disease
    Study Start Date :
    Oct 1, 2011
    Anticipated Primary Completion Date :
    Oct 1, 2013
    Anticipated Study Completion Date :
    Oct 1, 2013

    Outcome Measures

    Primary Outcome Measures

    1. eGFR slope [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.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Pre dialysis clinic Dan Petach Tiqua county General health service Ganey Tiqua Israel 55900

    Sponsors and Collaborators

    • Benaya Rozen-Zvi

    Investigators

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

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Benaya Rozen-Zvi, attending nephrologist pre dialysis clinic Dan petach-tiqua county, Meir Medical Center
    ClinicalTrials.gov Identifier:
    NCT01423045
    Other Study ID Numbers:
    • UCONC
    First Posted:
    Aug 25, 2011
    Last Update Posted:
    Aug 25, 2011
    Last Verified:
    Aug 1, 2011
    Keywords provided by Benaya Rozen-Zvi, attending nephrologist pre dialysis clinic Dan petach-tiqua county, Meir Medical Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 25, 2011