Trial for Prevention of Contrast Nephropathy With Sodium Bicarbonate

Sponsor
Kaiser Permanente (Other)
Overall Status
Completed
CT.gov ID
NCT00312117
Collaborator
(none)
300
1
1
294.6

Study Details

Study Description

Brief Summary

Contrast nephropathy (CN) is a common cause of renal failure associated with prolonged hospitalization, significant morbidity/mortality, and cost. In addition, these patients may require temporary or permanent hemodialysis which, in turn, is associated with further morbidity, mortality, and cost. CN has been reported to account for 10% of hospital acquired renal failure. In recent years, studies have investigated preventive therapies with mixed results. Fenoldopam was found to be ineffective in a large randomized trial. Dopamine has been shown to be ineffective as a preventive strategy. Hemofiltration has been shown to be beneficial (New England Journal of Medicine [NEJM] 2003) but is costly and not practical. Mucomyst has shown mixed results. The single strategy which most would agree as being beneficial remains hydration, most commonly with intravenous 0.9% normal saline. Most recently, sodium bicarbonate has been shown to be beneficial in a small randomized trial (n=119). It is clear that the most cost effective strategies for treatment of CN should be aimed at prevention.

The general question is: "Is a sodium bicarbonate solution more efficacious in preventing contrast nephropathy compared to normal saline?" The general hypothesis is that sodium bicarbonate will be more efficacious.

Condition or Disease Intervention/Treatment Phase
  • Drug: Sodium bicarbonate
Phase 3

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Official Title:
A Randomized Trial for Prevention of Contrast Nephropathy With Sodium Bicarbonate
Study Start Date :
Jan 1, 2006
Actual Study Completion Date :
Feb 1, 2006

Outcome Measures

Primary Outcome Measures

  1. development of contrast induced nephropathy, defined by a decrease in glomerular filtration rate (GFR) by 25% or more []

Secondary Outcome Measures

  1. change in serum creatinine []

  2. difference in hospital duration between groups []

  3. need for hemodialysis []

  4. 30 day mortality []

  5. difference of baseline to lowest GFR and highest creatinine between groups []

  6. difference in GFR and creatinine from baseline and 2-8 weeks later []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • GFR < 60 mL/min/1.73m2. GFR will be adjusted by a correction factor as reported by our laboratory for patients self identifying as black.

  • 18 years and have at least one of the following risk factors for contrast nephropathy: diabetes (type 2), congestive heart failure, hypertension (> 140/90), or age > 75.

  • Both inpatients and outpatients will be offered enrollment.

Exclusion Criteria:
  • Patients unable to give consent

  • Already receiving sodium bicarbonate solution

  • Undergoing emergency cardiac catheterization

  • Receiving a contrast agent other than Oxilan

  • On hemodialysis

  • Recent exposure to contrast within 2 days

  • Pulmonary edema

  • Active congestive heart failure

  • Severe valvular abnormality

  • Recent significant change in kidney function (> 15% over 2d)

  • One kidney

  • Kidney transplant status

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kaiser Permanente Medical Center Los Angeles California United States 90027

Sponsors and Collaborators

  • Kaiser Permanente

Investigators

  • Principal Investigator: Somjot S Brar, M.D., Kaiser Permanente

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Kaiser Permanente
ClinicalTrials.gov Identifier:
NCT00312117
Other Study ID Numbers:
  • 4353
First Posted:
Apr 7, 2006
Last Update Posted:
Mar 11, 2015
Last Verified:
Mar 1, 2015
Keywords provided by Kaiser Permanente
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 11, 2015