Actively Recruiting

Age: 18Years +
All Genders
ID07631221

Effect of Protein Dosage on Persistent Acute Renal Failure in Critically Ill Patients

Led by Hospital Italiano de Buenos Aires · Updated on 2026-06-05

344

Participants Needed

6

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Acute kidney injury (AKI) is a common and serious condition in critically ill patients, often leading to longer intensive care stays, the need for dialysis, and higher risk of death. This research evaluates whether critically ill patients with AKI who receive a higher protein intake (more than 1.2 grams per kilogram per day) have different outcomes compared to those receiving standard or lower protein intake (1.2 grams/kg/day or less). The study uses a retrospective design to analyze existing patient data from multiple hospitals in Argentina. Patients are classified into two groups based on their protein intake recorded on the fifth day of ICU admission: one group with standard protein intake (1.2 g/kg/day or less) and another with high protein intake (greater than 1.2 g/kg/day). No new treatments or interventions are given as part of the study; it involves reviewing medical records from patients who received exclusive enteral or parenteral nutrition. The study focuses on adults aged 18 and older with AKI or worsening chronic kidney disease according to specific criteria. Participants' kidney function recovery time within 30 days is the primary outcome, measured by a return of creatinine levels close to baseline. Secondary outcomes include changes in blood urea levels, duration of renal replacement therapy, length of ICU stay, and 30-day mortality. Advanced statistical methods will adjust for differences between groups to fairly compare outcomes. The study involves no direct participant procedures and uses only de-identified retrospective data, with confidentiality maintained according to local laws.

CONDITIONS

Brief Title

Effect of Protein Dosage on Persistent Acute Renal Failure in Critically Ill Patients.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years or older admitted to the ICU
  • Receiving exclusive enteral or parenteral nutrition
  • Diagnosis of acute kidney injury or worsened chronic kidney disease according to KDIGO criteria
Not Eligible

You will not qualify if you...

  • Chronic kidney disease with creatinine clearance less than 30 ml/min/1.73 m2 or on dialysis at admission
  • History of kidney transplantation
  • Severe liver disease with Child-Pugh score greater than 7
  • Acute kidney injury requiring renal replacement therapy at baseline
  • Body mass index greater than 30

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 30 days from ICU day 5 (Time Zero) or until ICU discharge, whichever occurs first.

Participants who are critically ill and have acute kidney injury are observed retrospectively to assess their protein intake and kidney function outcomes.

Data is collected from electronic health records without additional visits

Trial Site Locations

Total: 6 locations

1

Clinica Bazterrica

Buenos Aires, Buenos Aires, Argentina

Not Yet Recruiting

2

Hospital Alemán

Buenos Aires, Buenos Aires F.D., Argentina, C1118AAT

Not Yet Recruiting

3

Hospital Italiano de Buenos Aires

Buenos Aires, Buenos Aires F.D., Argentina, C1199ABB

Actively Recruiting

4

Hospital Privado Universitario de Córdoba

Córdoba, Córdoba Province, Argentina, X5016KEH

Actively Recruiting

5

Hospital Universitario Austral

Buenos Aires, Pilar, Argentina, B1629AHJ

Actively Recruiting

6

Hospital Italiano sede San Justo Agustín Rocca

Buenos Aires, San Justo, Argentina, C1198AAW

Actively Recruiting

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Research Team

I

Ivan Alfredo Huespe, MS

V

Veronica Ester Monzon, MS

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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