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Prevention of Contrast-induced Nephropathy in Patients With Acute Myocardial Infarction

Prevention of Contrast-induced Nephropathy in Patients With Acute Myocardial Infarction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01160627
Enrollment
720
Registered
2010-07-12
Start date
2010-04-30
Completion date
2013-03-31
Last updated
2013-03-22

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

Conditions

Contrast Induced Nephropathy

Keywords

CIN STEMI

Brief summary

OBJECTIVE: To evaluate the efficacy of prevention of contrast induced nephropathy in patients with ST segment elevation myocardial infarction treated with primary percutaneous coronary intervention. DESIGN: Prospective study. SETTING: Three-center study Acute kidney injury was defined as a rise in creatinine \>25% from baseline Serum creatinine will be measured at baseline and each day for the following 3 days and at 30 days. Patients will be randomised to: 1. Standard treatment 2. Standard treatment + acetylcystein for 2 days 3. Standard treatment + Sodium bicarbonate 500 ml / followed by 100 ml/h for 5 hours 4. Standard treatment + acetylcystein for 2 days + Sodium bicarbonate 500 ml / followed by 100 ml/h for 5 hours

Interventions

OTHERHydration

Saline hydration

DRUGAcetylcysteine

Acetylcystein tablets for 2 days

DRUGSodium bicarbonate

Sodium bicarbonate 500 ml followed by 100 ml/hour for 5 hours

DRUGCombined Acetylcystein and Sodium Bicarbonate

Sodium bicarbonate 500 ml followed by 100 ml/hour for 5 hours combined with acetylcystein tablets for 2 days

Sponsors

Odense University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* STEMI patients treated with primary PCI

Exclusion criteria

* Cardiogenic shock

Design outcomes

Primary

MeasureTime frameDescription
Prevention of contrast induced nephropathy in STEMI patients treated with primary PCIfrom baseline to day 3Rise in creatinine \>25% from baseline to day 3

Secondary

MeasureTime frameDescription
Prevention of contrast induced nephropathy in STEMI patients treated with primary PCIfrom baseline to day 30Rise in creatinine \>25% from baseline to day 30

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026