NCT07235891Not yet recruitingPhase 4
Retinal Protective Effects of Novel Finerenone in Patients With Chronic Kidney Disease
Investigating the Impact of Finerenone on Retinal Vascular Dysfunction in Patients With Chronic Kidney Disease
Source: ClinicalTrials.gov · Last updated 19 Nov 2025
Brief summary (registry, in English)
Interestingly, A hypothesis-generating analysis was conducted from two studies using routine ophthalmological examinations from clinical trial participants (ReFineDR/DeFineDR), suggesting a potential benefit of finerenone in the delay of progression of non-proliferative diabetic retinopathy (NPDR), independent of baseline HbA1c. Potential benefits of finerenone were also observed in the prevention of required ocular interventions. However, the studies relied on routine ophthalmological examinations done retrospectively, which may have affected data quality and certainly affected quantity. Hence, there is a compelling need to conduct randomized studies with adequate power to detect a potential benefit of finerenone in delaying retinopathy progression, particularly given the lack of alternative options for oral treatment of retinopathy.
- Status (registry)
- Not yet recruiting
- Phase (registry)
- Phase 4
- Study type
- Interventional
- Enrollment
- 40 (estimated)
- First submitted
- 16 Sept 2025
- Start date
- 20 Nov 2025
- Primary completion date
- 20 Dec 2026
- Lead sponsor
- Alexandria University
- Diseases
- Chronic kidney disease
- NCT number
- NCT07235891
What you commit to
- Study type: Interventional · Phase 4
- Planned participants: 40
- From 20 Nov 2025 to the primary completion date, 20 Dec 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Prior/planned ocular interventions (retinal laser treatment, intravitreal injection or vitrectomy).
Other illness
- Malignancy
Lab values
- Serum potassium level \> 5.5 mEq/L
Other
- Patients on hemodialysis (HD).
- Pregnant and lactating women
Who the study is looking for
- Age: above 18 years
- Diabetic and non-diabetic non-hemodialysis CKD patients (Stage 2 - Stage 4).
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Alexandria university Coordinator of this site? Confirm its status | Alexandria | Egypt | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.