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AC/DC Study: Acidification test in patients with Chronic kidney Disease and healthy Controls

AC/DC Study: Acidification test in patients with Chronic kidney Disease and healthy Controls - AC/DC study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON42898
Enrollment
24
Registered
2016-10-07
Start date
2017-03-27
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic kidney disease chronic renal insufficiency

Interventions

All participants will undergo a urinary acidification test with ammonium chloride.

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with CKD: - Male or female adults (*18 years) - Chronic kidney disease stage 4 (eGFR: 15-30 ml/min/1.73 m2) Healthy subjects: - Healthy male or female adults (* 18 years) - Normal kidney function (eGFR > 90 ml/min/1.73 m2)

Exclusion criteria

Exclusion criteria: Patients with CKD: - Plasma bicarbonate level 5.5 mmol/l - Sodium bicarbonate use in the month preceding the study - 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-hypertensives - Kidney transplantation - Use of calcineurin inhibitors - 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 subjects: - eGFR

Design outcomes

Primary

MeasureTime frame
The primary study parameter is the change in urinary renin values (an accepted measure of intrarenal RAS activity).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)