Overview

The Effect of Curcumin Against Colistin-induced Nephrotoxicity

Status:
Recruiting
Trial end date:
2024-09-30
Target enrollment:
0
Participant gender:
All
Summary
The goal of this study is to investigate the possible nephroprotective effect of curcumin in critically ill patients receiving colistin.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
October 6 University
Collaborator:
Cairo University
Treatments:
Colistin
Curcumin
Criteria
Inclusion Criteria:

- All critically ill adult patients (18-65 years old) who are infected by MDR
Gram-negative bacteria and require intravenous colistin therapy

Exclusion Criteria:

- Patients receiving intravenous colistin therapy for < 72 hours.

- Patients receiving renal replacement therapy (RRT).

- Patients with diseases that may contribute to renal impairment such as systemic lupus
erythematosus, acute myocardial infarction, cancer, HIV infection,
glucose-6-phosphate-dehydrogenase deficiency, or urinary tract stone.

- Pregnancy or breastfeeding.

- Known allergy to the study medications.

- Patients with chronic kidney diseases (creatinine clearance < 60 mg/dL).

- Elevated total liver enzymes (AST, and ALT) three times above the upper limit of
normal.

- Patients with acute decompensated heart failure signs and symptoms requiring
intravenous loop diuretics and/or intravenous inotropes and/or ACE inhibitors.

- Uncontrolled diabetes (Glycosylated hemoglobin (Hb A1C) >8%).

- Hypotensive patients defined as decrease in blood pressure less than 90/60 mm Hg.

- Recent use of vitamins with antioxidant properties such as beta carotene, vitamin E,
vitamin C, selenium, or N-acetylcysteine or any other medications known to have
nephroprotective activities.

- Patients receiving other nephrotoxic drugs at enrollment (e.g., aminoglycosides,
vancomycin, or amphotericin B) or administration of contrast medium within 7 days.