Clinical Trial Details
— Status: Recruiting
Administrative data
NCT number |
NCT05105009 |
Other study ID # |
19-1131 |
Secondary ID |
|
Status |
Recruiting |
Phase |
Phase 3
|
First received |
|
Last updated |
|
Start date |
March 3, 2020 |
Est. completion date |
July 1, 2022 |
Study information
Verified date |
October 2021 |
Source |
Instituto Nacional de Cardiologia Ignacio Chavez |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial 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.
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.