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NCT07368712

A Methodological Study to Learn More About Kidney Function in Healthy People and in People With Reduced Kidney Function

Recruiting now NA Last updated 17 April 2026
What this trial tests

NA trial testing No investigational study intervention in Acute Kidney Injury, Renal Insufficiency in 50 participants. Currently enrolling.

Timeline
6 January 2026
Primary endpoint
19 February 2027
19 February 2027

Quick facts

Lead sponsorBayer
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment50
Start date6 January 2026
Primary completion19 February 2027
Estimated completion19 February 2027
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

Bayer — full company profile →

Who can join

Adults 18 to 75, any sex, with Acute Kidney Injury, Renal Insufficiency. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The main purpose of this study is to investigate how reliable a test assessing the renal functional reserve (RFR) and the maximum glomerular filtration rate (maxGFR) are. MaxGFR and RFR assessments are repeated twice at 1-month intervals. If precise, this test may improve the measure of kidney function and be useful in future studies for people with chronic kidney problems. To do this, the researchers will collect and analyze information about kidney function from up to 50 adults, including healthy people and people with stable kidney problems. Each person will come to the study center for a screening visit and then three study days, each about a month apart. On each study day, participants will have blood and urine samples taken before and after drinking a protein shake. The tests will measure things like creatinine, cystatin C, and other markers in the blood and urine to see how the kidneys are working. The study will also record basic health information, weight, blood pressure, and any medicines being taken. The study will last about 2 to 2.5 months for each participant.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of No investigational study intervention

Trials testing the same drug.

Other Bayer trials

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07368712.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing