Finerenone for IgA-Nephropathy Treatment Trial
This trial is investigating whether finerenone can improve kidney function in patients with IgA-Nephropathy, a kidney disorder, by measuring changes in albuminuria levels.
Finerenone
Urogenital Diseases+8
+ Autoimmune Diseases
+ Female Urogenital Diseases and Pregnancy Complications
Treatment Study
Summary
Study start date: May 21, 2025
Actual date on which the first participant was enrolled.IgA nephropathy is a common kidney condition known for its poor outlook when persistent albuminuria is present. This study focuses on the drug finerenone, which has shown promise in lowering albumin levels in people with chronic kidney disease (CKD) and type 2 diabetes. The trial aims to explore finerenone's potential benefits for patients with IgA nephropathy, a type of non-diabetic kidney disease. By examining its effects beyond standard treatments, the study hopes to determine if finerenone can slow down the progression of kidney damage in these patients. Participants in this study will receive finerenone in addition to their regular treatment. Researchers will monitor for any side effects and assess the drug's ability to protect the kidneys. The study does not specify the exact methods of finerenone administration, but its results will be measured by observing changes in kidney function and the occurrence of any adverse events. This could lead to new insights into managing IgA nephropathy and improving outcomes for those affected.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.30 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.3 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalGroup III
ExperimentalStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location