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Completed

NCT Number: NCT03293446

AC/DC Study: Acidification Test in Patients With Chronic Kidney Disease and Healthy Controls

In this study the effect of an acute acid load on the intrarenal renin angiotensin-system is evaluated in patients with chronic kidney disease and healthy controls

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Key information

Age range

18 year–99 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Erasmus MC

Rotterdam, South Holland, 3015CN, Netherlands

About this study

Metabolic acidosis is one of the metabolic complications of chronic kidney disease (CKD). Correction of metabolic acidosis in CKD has been shown to prevent further loss of kidney function over time. Currently, a clinical trial (the BIC-study, MEC-2013-332) is conducted in which patients with CKD and metabolic acidosis receive sodium bicarbonate, sodium chloride, or no treatment (time control) to address the hypothesis that the beneficial effects of acidosis correction are mediated through inhibition of the intrarenal renin-angiotensin system (RAS). It is unknown, however, if and how acute changes in acid-base status affect the intrarenal RAS during CKD. In the present study it is hypothesized that an acute acid load increases the activity of the intrarenal RAS, and that this response is exaggerated in patients with CKD compared with healthy controls.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Patients with CKD:

  • Male or female adults (≥18 years)
  • Chronic kidney disease stage 4 (eGFR: 15-30 ml/min/1.73 m2, calculated using the CKD-EPI equation)

Healthy controls:

  • Healthy male or female adults (≥ 18 years)
  • Normal kidney function (eGFR > 90 ml/min/1.73 m2, calculated using the CKD-EPI equation)

Exclusion criteria

  • CKD patients
  • Plasma bicarbonate level < 20.0 mmol/l
  • Serum potassium >5.5 mmol/l
  • Sodium bicarbonate use in the month preceding the test
  • Heart failure (NYHA III or IV)
  • Liver cirrhosis (Child Pugh B or C)
  • Blood pressure >140/90 mmHg despite the use of 3 different anti-hypertensive drugs
  • Kidney transplantation
  • Use of calcineurin inhibitors (these immunosuppressive drugs affect acid-base balance)
  • Known urea cycle disorder
  • Alcoholism or drug use
  • Pregnancy
  • Current use of antibiotics, NSAIDS or alkalizing drugs (sodium-bicarbonate, citric acid, potassium citrate, acetazolamide)
  • Inability to adhere to the study protocol (due to language barrier or intellectual disability)

Healthy controls:

  • eGFR < 90 ml/min/1.73 m2 (calculated using the CKD-EPI equation)
  • Plasma bicarbonate < 20 mmol/l
  • History of, or drugs for, diabetes mellitus
  • History of chronic diarrheal disease
  • Ileostomy/colostomy
  • Known urea cycle disorder
  • Alcoholism or drug use
  • Pregnancy
  • Current use of antibiotics, antihypertensive drugs, NSAIDS or alkalizing drugs (sodium-bicarbonate, citric acid, potassium citrate, acetazolamide)
  • Inability to adhere to the study protocol (due to language barrier or intellectual disability)

Treatment and study plan

Urinary acidification test

Diagnostic Test

Urinary acidification by administration of ammonium chloride (100 mg/kg body weight, given orally) during a single-day hospital admission.

Primary outcomes

  1. Urinary renin

    Time frame: up to 6 hours

Sponsors and collaborators

Lead sponsor

Erasmus Medical Center

Other

Registry information

Acronym: AC/DC

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Sep 26, 2017
Registry last updated
Jun 20, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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