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Efficacy Trial of N-Acetylcysteine and Sodium Bicarbonate for the Prevention of Contrast-Induced Acute Kidney Injury (PREKIT)

Primary Purpose

Chronic Kidney Disease

Status
Unknown status
Phase
Phase 3
Locations
Japan
Study Type
Interventional
Intervention
Physiological Saline, N-Acetylcysteine and Sodium Bicarbonate
Sponsored by
Tokushukai Medical Group
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Chronic Kidney Disease focused on measuring Chronic Kidney Disease, Contrast Media, Acute Kidney Injury, N-Acetylcysteine, Bicarbonate

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • serum creatinine more or equal than 1.1mg/dL
  • procedures using contrast media

Exclusion Criteria:

  • congestive heart failure
  • serum creatinine less than 1.1mg/dl
  • allergy to contrast media
  • preexisting dialysis
  • emergency catheterization
  • recent exposure to contrast within 2 days of the study
  • refuse to entry this study
  • PTRA
  • dialysis after procedure

Sites / Locations

  • Sapporo Higashi Tokushukai Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Physiological Saline and N-Acetylcysteine

Physiological Saline, N-Acetylcysteine and Sodium Bicarbonate

Arm Description

Outcomes

Primary Outcome Measures

Development of contrast-induced acute kidney injury
Contrast-Induced Acute Kidney Injury(CIAKI) was defined as an absolute increase in serum creatinine of more than or equal to 0.3mg/dl (≥ 26.4 μmol/l), a percentage increase in serum creatinine of more than or equal to 50% (1.5-fold from baseline) within 48 hours of intravascular contrast administration in the absence of any alternative causes, or a reduction in urine output documented oliguria of less than 0.5 ml/kg per hour for more than six hours.

Secondary Outcome Measures

Requirement of dialysis
Requirement of hospitalization and death

Full Information

First Posted
July 11, 2010
Last Updated
September 13, 2014
Sponsor
Tokushukai Medical Group
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1. Study Identification

Unique Protocol Identification Number
NCT01210456
Brief Title
Efficacy Trial of N-Acetylcysteine and Sodium Bicarbonate for the Prevention of Contrast-Induced Acute Kidney Injury
Acronym
PREKIT
Official Title
The Prevention Contrast-Induced Acute Kidney Injury With the Triple Combination of Hydration With Physiological Saline, N-Acetylcysteine and Sodium Bicarbonate
Study Type
Interventional

2. Study Status

Record Verification Date
September 2014
Overall Recruitment Status
Unknown status
Study Start Date
October 2009 (undefined)
Primary Completion Date
October 2014 (Anticipated)
Study Completion Date
November 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tokushukai Medical Group

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Contrast-Induced Acute Kidney Injury(CIAKI) was defined as an absolute increase in serum creatinine of more than or equal to 0.3mg/dl (≥ 26.4 μmol/l), a percentage increase in serum creatinine of more than or equal to 50% (1.5-fold from baseline) within 48 hours of intravascular contrast administration in the absence of any alternative causes, or a reduction in urine output documented oliguria of less than 0.5 ml/kg per hour for more than six hours. It is the common cause of new hospital-acquired renal insufficiency. The occurrence of CIAKI may be influenced by pre-existing renal insufficiency, diabetic nephropathy, dehydration, congestive heart failure, concurrent administration of nephrotoxic drugs, or the dose and type of contrast media used. Previous studies have shown the independent effectiveness of several agents in preventing CIAKI. Even now, hydration is crucial for preventing CIAKI. Since CIAKI is presumed to be caused by free radical generation, N-Acetylcysteine, which is a potent free radical scavenger, is shown to be effective in preventing nephropathy. At the same time, because free radical formation is promoted by an acidic environment, bicarbonate, which alkalinizes renal tubular fluid, has been shown to reduce renal involvement. These days, some studies have shown that hydration with sodium bicarbonate plus N-Acetylcysteine was effective and safe in the prevention of CIAKI. In these studies, bicarbonate was used for both alkalinizing renal tubular fluid and hydration. However, if we want to do hydration, we can use saline and if we want to alkalinize renal tubular fluid, we might use bicarbonate by bolus injection. Actually, bicarbonate for hydration is prepared at sterile preparation room in a hospital, which is very cumbersome procedure and increase in cost. This is one of the reasons that bicarbonate for hydration use does not become common with wide clinical application. In past issues, though it differs depending on the level of the renal dysfunction, the probability of CIAKI was 8-33% when hydration was administered, 5-15% when hydration and N-Acetylcysteine were administered, and 1.8-1.9% when bicarbonate and N-Acetylcysteine were administered. Thus, we can hypothesize the combination of N-Acetylcysteine and bicarbonate will play a complementary role in preventing contrast-induced nephropathy. This is the rational for this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease
Keywords
Chronic Kidney Disease, Contrast Media, Acute Kidney Injury, N-Acetylcysteine, Bicarbonate

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
458 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Physiological Saline and N-Acetylcysteine
Arm Type
Active Comparator
Arm Title
Physiological Saline, N-Acetylcysteine and Sodium Bicarbonate
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Physiological Saline, N-Acetylcysteine and Sodium Bicarbonate
Intervention Description
All patients receive N-Acetylcysteine(NAC) and sodium chloride. NAC is given orally at a dose of 700mg twice daily, on the day before and on the day of administration of the contrast media, for a total of two days. 154mEq/L of sodium chloride is given intravenously. The initial intravenous bolus is 3ml/kg per hour for 1 hour immediately before contrast injection. And then, patients receive the same fluid at 1ml/kg per hour during the contrast exposure and for 6 hours after the procedure. In addition, intervention arms receive sodium bicarbonate.1000mEq/L of sodium bicarbonate is given intravenously twice at a dose of 40ml immediately before the contrast exposure and immediately after the procedure.
Primary Outcome Measure Information:
Title
Development of contrast-induced acute kidney injury
Description
Contrast-Induced Acute Kidney Injury(CIAKI) was defined as an absolute increase in serum creatinine of more than or equal to 0.3mg/dl (≥ 26.4 μmol/l), a percentage increase in serum creatinine of more than or equal to 50% (1.5-fold from baseline) within 48 hours of intravascular contrast administration in the absence of any alternative causes, or a reduction in urine output documented oliguria of less than 0.5 ml/kg per hour for more than six hours.
Time Frame
within 48 hours
Secondary Outcome Measure Information:
Title
Requirement of dialysis
Time Frame
6 months
Title
Requirement of hospitalization and death
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: serum creatinine more or equal than 1.1mg/dL procedures using contrast media Exclusion Criteria: congestive heart failure serum creatinine less than 1.1mg/dl allergy to contrast media preexisting dialysis emergency catheterization recent exposure to contrast within 2 days of the study refuse to entry this study PTRA dialysis after procedure
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daisuke Hachinohe, MD
Organizational Affiliation
Sapporo Higashi Tokushukai Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sapporo Higashi Tokushukai Hospital
City
Sapporo City
State/Province
Hokkaido
ZIP/Postal Code
065-0033
Country
Japan

12. IPD Sharing Statement

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Efficacy Trial of N-Acetylcysteine and Sodium Bicarbonate for the Prevention of Contrast-Induced Acute Kidney Injury

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