No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
198 (estimated)
Sponsor
Gaziosmanpasa Research and Education Hospital · Government
Who this trial is looking for
This trial is looking for adults who are at risk for kidney injury due to contrast dye used in CT scans. Participants will either receive hydration through an IV or drink water, depending on their group assignment.
Are You a Good Fit for This Trial?
You may be able to join if
I am 18 years or older.
I have an estimated kidney function (eGFR) between 15-59.
I need a contrast-enhanced CT scan in the emergency department.
I have signed and given my consent to participate.
You may not be able to join if
I am pregnant.
I have end-stage renal disease or receive dialysis.
I have heart failure that is not under control.
I am allergic to contrast dye.
I have had contrast exposure in the last 72 hours.
I cannot take anything by mouth.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
This study is planned to be conducted by emergency physicians between November 7, 2025, and December 7, 2026.
Inclusion and Exclusion Criteria The study will include adult patients aged 18 years and older who are considered at risk for Contrast-Associated Acute Kidney Injury (CA-AKI), with an estimated Glomerular Filtration Rate (eGFR) between 15-59 ml/min/1.73 m², a clinical indication for contr…
This study is planned to be conducted by emergency physicians between November 7, 2025, and December 7, 2026.
Inclusion and Exclusion Criteria The study will include adult patients aged 18 years and older who are considered at risk for Contrast-Associated Acute Kidney Injury (CA-AKI), with an estimated Glomerular Filtration Rate (eGFR) between 15-59 ml/min/1.73 m², a clinical indication for contrast-enhanced CT, and who have provided signed informed consent.
Exclusion criteria are as follows:
Pregnant women.
Patients with a known contrast media allergy.
Contrast media exposure within the last 72 hours.
End-stage renal disease (ESRD) with eGFR \<15 ml/min/1.73 m² or those receiving dialysis.
Patients with clinical decompensated heart failure.
Patients for whom oral intake is contraindicated or not tolerated.
Randomization and Interventions Prior to randomization, the oral intake capacity of eligible patients will be verified. Participants will be randomized into two groups-IV hydration and oral hydration-at a 1:1 ratio using stratified block randomization based on age and gender.
IV Hydration Group: Isotonic 0.9% NaCl solution will be administered. The regimen consists of 3 ml/kg for 1 hour pre-procedure, followed by 2 ml/kg/hour for 4 hours post-procedure. Patients with an ejection fraction (EF) \<40% will receive half-doses (1.5 ml/kg pre-procedure; 1 ml/kg/hour for 4 hours post-procedure).
Oral Hydration Group: Drinking water will be administered under nursing supervision. The regimen consists of 500 ml 1 hour pre-procedure and 125 ml/hour for 4 hours post-procedure. Patients with an EF \<40% will receive half-doses (250 ml pre-procedure; 62.5 ml/hour post-procedure).
Follow-up and Outcome Measures Baseline renal function tests will be obtained from all patients prior to the protocol. Patients will be re-evaluated for CA-AKI via blood samples taken 48-72 hours after contrast administration.
Furthermore, eGFR changes will be calculated using the Modification of Diet in Renal Disease (MDRD) formula. Mehran Risk Scores will also be determined for each patient. Long-term outcomes, including progression to ESRD (requirement for dialysis) and mortality within 1 month, as well as creatinine levels between days 30-45, will be assessed.
Trial Locations
Loading…
Loading trial locations…
Facility
City
State
Country
Status
Eligibility Criteria
Inclusion Criteria:
* Patients aged 18 years and older.
* Patients with an estimated Glomerular Filtration Rate (eGFR) between 15-59 mL/min/1.73 m².
* Patients undergoing contrast-enhanced computed tomography (CT) in the emergency department.
* Patients who have provided written informed consent.
…
Inclusion Criteria:
* Patients aged 18 years and older.
* Patients with an estimated Glomerular Filtration Rate (eGFR) between 15-59 mL/min/1.73 m².
* Patients undergoing contrast-enhanced computed tomography (CT) in the emergency department.
* Patients who have provided written informed consent.
Exclusion Criteria:
* Pregnant women.
* Patients with end-stage renal disease (ESRD) receiving dialysis or those with an eGFR \<15 mL/min/1.73 m².
* Patients presenting with decompensated heart failure.
* Patients with a known allergy to iodinated contrast media.
* Patients with contrast media exposure within the last 72 hours.
* Patients for whom oral intake is contraindicated or who cannot tolerate oral intake
Contacts
No contact information available.
What are you hoping to find?
Picking one helps us show the most relevant trials first.
Your results are loading in the background — you can
change this any time from the results page.
Set your location to continue
Find My Trials uses your location to surface clinical trials near you.
Add your city or zip code to your profile and try again.