Furosemide and Creatinine Tubular Stress Test in Order to Measure Proximal Tubule Residual Function

Sponsor
Instituto Nacional de Cardiologia Ignacio Chavez (Other)
Overall Status
Recruiting
CT.gov ID
NCT05105009
Collaborator
(none)
72
1
2
27.9
2.6

Study Details

Study Description

Brief Summary

This is a two phase study. The first part will take place at the National Institute of Cardiology in Mexico, the second phase will be made in collaboration with the University of California San Diego.

This is a non blind experimental study, 60 patients with different stages of CKD from the outpatient unit of the institute will be included. Each patient will receive a furosemide stress test of 1 mg/kg in non diuretic users and 1.5 mg/kg in diuretic users, in addition to an oral load of 5 grams of creatinine, as well as Iohexol to measure GFR. After the intervention blood and urine samples will be drawn at 10 minutes, 30 minutes, and every hour until the completion of the observation at 6 hours.

Blood and urine will be analized to measure creatinine (blood and urine), then samples will be processed for measurement of furosemide (mass spectometry), indoxyl sulphate, p-cresol, hippurate, and uromoduline.

The aim of this stiudy is to asses the differences between GFR and proximal tubule function.

Condition or Disease Intervention/Treatment Phase
Phase 3

Detailed Description

Residual kidney function (RKF) its a critical tool in the CKD evolution and prognosis. It's well known that preserving RKF increases survival in patients with CKD.

Traditionally Glomerular Filtration Rate (GFR), and proteinuria have been the variables used to asses RKF, wich are glomerular residual function (GRF) variables. This glomerulocentric assestment of RKF has been challenged recently. It is knows that urea is not the principal uremic toxine, the protein boud uremic toxins are particullary important because it's elimination depends of the proximal tubular organic anionic transporters (OAT), and the organic cationic transporters (OCT). The functional integrity of this transporters are lost in advanced CKD stages, and it´s accumulation increases cardiovascular and renal damage because they activate proinflammatory citokines, increasing mortality, this was shown specially with the accumulation and clearance of hippurate and p-cresol independently of GFR.

The purpose of this study is to asses the functional capacity of two AOT (hOAT1, and hOAT3, that can be blocked by furosemide), and one OCT (OCT2 blocked by creatinine) using an stress test. The stress test will be performed in healthy subjects as well as in CKD from different stages. Protein bound uremic toxins such as indoxyl sulphate, p-cresol, and hippurate will be measured.

In the stress the typical furosemide stress test described previously by Mehta will be implemented, in addition to an oral load of 5 grams of creatinine oral load. This levels should be efficient enough to assess the functionality of the OCT2. A comparison between the tubular creatinine secretine to filtrated creatinine measuring GFR using Iohexol will be performed.

In conclusion this is a pilot study aimed to establish a practical methodology for the assesment of proximal tubular function.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
72 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
CKD Cohort with and control group of healthy kidney donors.CKD Cohort with and control group of healthy kidney donors.
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Furosemide and Creatinine Tubular Stress Test in Order to Measure Proximal Tubule Residual Function: Is it Better Than GFR?
Actual Study Start Date :
Mar 3, 2020
Anticipated Primary Completion Date :
Dec 1, 2021
Anticipated Study Completion Date :
Jul 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Healthy Kidney Donors

12 Healthy Kidney Organ Donors

Drug: Furosemide
Furosemide Stress Test ( 1mg/kg in non diuretic users and 1.5 mg/kg in diuretic users). Oral creatinine load using 5 grams of creatinine
Other Names:
  • Creatinine
  • Experimental: CKD Patients

    12 patients for each CKD Stage

    Drug: Furosemide
    Furosemide Stress Test ( 1mg/kg in non diuretic users and 1.5 mg/kg in diuretic users). Oral creatinine load using 5 grams of creatinine
    Other Names:
  • Creatinine
  • Outcome Measures

    Primary Outcome Measures

    1. Tubular Residual Kidney Function [1 year]

      To assess the functionallity of the HOAT1 and 3, as well OCT2 by stress test using furosemide and creatinine loads

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Patients older than 18 years old.

    • Patients with CKD that attends to the outpatient clinic.

    • Residual uresis of 500 mL

    Exclusion Criteria:
    • Patients younger than 18 years old.

    • Increase of Cr in a rate of 0.5 mg/dL, or loss of more than 30% of previous GFR.

    • Patients with cardiorrenal syndrome type 1.

    • Patients with dilated miocardiopathy.

    • Volume overload.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Instituto Nacional de Cardiologia Ignacio Chávez Mexico City Mexico 14080

    Sponsors and Collaborators

    • Instituto Nacional de Cardiologia Ignacio Chavez

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Magdalena Madero, Head of Nephrology, Instituto Nacional de Cardiologia Ignacio Chavez
    ClinicalTrials.gov Identifier:
    NCT05105009
    Other Study ID Numbers:
    • 19-1131
    First Posted:
    Nov 3, 2021
    Last Update Posted:
    Nov 3, 2021
    Last Verified:
    Oct 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 3, 2021