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Fluorescein Angiography in Patients With Diabetes and Chronic Kidney Disease

Fluorescein-Induced Acute Kidney Injury in Patients With Diabetes and Chronic Kidney Disease

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06760650
Acronym
Fluo-AKI
Enrollment
35
Registered
2025-01-07
Start date
2025-01-07
Completion date
2025-10-10
Last updated
2025-01-07

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

Conditions

Chronic Kidney Disease Stage 4, Chronic Kidney Disease Stage 3B, Chronic Kidney Disease Stage 5, Diabetes Mellitus, Fluorescein Angiography, Acute Kidney Injury

Keywords

Fluorescein Angiography, Acute kidney injury, Chronic kidney disease, Diabetes

Brief summary

Our study hypothesizes that fluorescein exposure in diabetic patients with advanced chronic kidney disease results in deterioration of kidney function. It will therefore aim to evaluate the incidence of acute kidney injury induced by fluorescein in diabetic patients with CKD. The objective is to determine the incidence, severity and risk factors associated with this deterioration to improve the care of this specific population.

Detailed description

This study will assess the change in serum creatinine in patients with diabetes and advanced chronic kidney disease, after a fluorescein angiography. This is a before and after study that will include 35 patients from the department of ophtalmology over 6 months with a total follow-up for 3 months.

Interventions

Fluorescein angiography

Sponsors

Saint-Joseph University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* \>18 years old with type 2 or type 1 diabetes and chronic kidney disease stage 3b to 5 (eGFR\<45 mL/min/1.73 m2)

Exclusion criteria

* Patients who do not give their consent * Patients who are allergic to fluorescein * Patients who are on dialysis * Patients who had fever, vomiting, diarrhea or any dehydration 48 hours before the intervention * Patients who had a treatment modification one week before the intervention

Design outcomes

Primary

MeasureTime frameDescription
Change in serum creatinineAt day 4Change in serum creatinine from baseline to day 4

Secondary

MeasureTime frameDescription
Long-term change in serum creatinine3 monthsChange in serum creatinine from baseline to end of the third month

Countries

Lebanon

Contacts

Primary ContactMabel AOUN, M.D., M.P.H.
aounmabel@yahoo.fr+9613351588
Backup ContactAnthony NOHRA, Medical Student
anthony.nohra1@net.usj.edu.lb

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026