Skip to content

Lycopene nephroprotective effect in patients receiving vancomycin

Evaluation of the nephroprotective effect of lycopene in patients receiving vancomycin

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171030037093N37
Enrollment
60
Registered
2020-05-04
Start date
2020-04-28
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Vancomycin-induced nephrotoxicity. Toxic nephropathy, not elsewhere classified

Interventions

Intervention 1: Intervention group: For people in the case group, lycopene tablets 15 mg with vancomycin will be prescribed once a day. Intervention 2: Control group: For control group participants, p

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Serum creatinine levels less than 1.2 mg / dl at the start of the study Creatinine clearance (ClCr)> 90 ml / min upon admission Lack of underlying renal impairment such as glomerulonephritis, polycystic kidney disease, kidney stones, interstitial nephritis, renal artery stenosis and renal carcinoma Lack of underlying diseases causes kidney disorders such as diabetes mellitus and high blood pressure Hospital history and failure to receive other nephrotoxic drugs such as aminoglycosides, amphotericin B, cyclosporine, tacrolimus and furosemide, etc. Do not take other antioxidant supplements such as vitamins C and E.

Exclusion criteria

Exclusion criteria: History of acute kidney damage Lycopene allergy history History of injectable addiction

Design outcomes

Primary

MeasureTime frame
Serum creatinine. Timepoint: Before starting treatment, one day between treatments and 12 hours after the last dose of vancomycin on the tenth day of treatment. Method of measurement: Photometric.;Blood urea nitrogen. Timepoint: Before starting treatment, one day between treatments and 12 hours after the last dose of vancomycin on the tenth day of treatment. Method of measurement: Photometric.;Creatinine clearance. Timepoint: Before starting treatment, one day between treatments and 12 hours after the last dose of vancomycin on the tenth day of treatment. Method of measurement: Cockcroft-Gault formula.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomaye Haghighipour

Esfahan University of Medical Sciences

s_haghighipour@yahoo.com+98 31 3653 1498

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026