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WithdrawnNCT00621972Updated Sep 20, 2018

AV Fistula Salvage in Advanced CKD Using Sodium Bicarbonate Prophylaxis

An observational study in Acute Renal Failure, sponsored by MaineHealth. Withdrawn at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-09-20.

Sponsored by MaineHealth · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
0
Ages
18 Years and older
Sex
All
01

Study summary

This is an observational study assessing the impact of conventional dose iodinated contrast on the renal function of advanced chronic kidney disease patients undergoing arteriovenous fistula evaluation using a standard sodium bicarbonate prophylaxis protocol. In addition, this model allows for pre and post procedure measurements of kidney function, providing a unique opportunity to assess the utility of novel biomarkers for contrast-induced kidney injury.

Our primary hypothesis is that there will be no change in serum creatinine post-procedure when using a standard sodium bicarbonate prophylaxis protocol. Our secondary hypothesis is that there will be no change in urinary kidney-injury marker-1 (KIM-1) post-procedure using a standard sodium bicarbonate prophylaxis protocol. In addition, we will assess the impact of different patient characteristics on the development of contrast-induced kidney injury, such as diabetes, coronary artery disease, hypertension, and angiotensin converting enzyme inhibitor therapy.

Read the detailed description

The National Kidney Foundation publishes kidney disease outcome guidelines for improving care of the chronic kidney disease (CKD) patient. Regarding hemodialysis vascular access, the recommendation is for early placement of an arteriovenous fistula (AVF) to improve morbidity and mortality outcomes, specifically when the glomerular filtration rate is less than 25ml/min, corresponding to stage 4 and 5 CKD. Despite its advantages, the need for surveillance of the AVF to determine maturation for use and maintain optimal longevity requires the use of interventional procedures. While radiocontrast use can lead to acute, often reversible kidney injury, its use in AVF evaluation has renewed interest with the recent implication of gadolinium-enhanced MRI being associated with a rare disorder of skin swelling and induration called nephrogenic systemic fibrosis. CKD patients are particularly susceptible to long term adverse outcomes from contrast-induced kidney injury, with 1 year mortality in stage 4 and 5 CKD patients being 44% and 62%, respectively. While optimal fluid therapy to prevent contrast-induced kidney injury remains uncertain, several prospective randomized trials using sodium bicarbonate pretreatment have shown a lower incidence of contrast-related kidney injury compared to isotonic saline. Traditional markers of acute kidney injury, including serum creatinine, blood urea nitrogen, and creatinine clearance have been insensitive in differentiating contrast-induced kidney injury from other forms of renal injury. Kidney injury marker-1 (KIM-1) is a transmembrane receptor induced to very high levels in the proximal tubule of the nephron following ischemic and nephrotoxic injury. KIM-1 has been shown in a small cohort of patients to differentiate ischemic kidney injury from other forms of acute and chronic kidney disease.

02

Conditions studied

  • Acute Renal Failure

Keywords

  • acute renal failure
  • arteriovenous fistula
  • KIM-1
  • chronic kidney disease
03

In context

Renal Insufficiency

1,995 studies on the registry are indexed under Renal Insufficiency; 173 are open to participants now.

Browse Renal Insufficiency studies →

Lead sponsor

MaineHealth is the lead sponsor of 34 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Stage 4 and 5 chronic kidney disease patients with AV fistula placed but have not initiated dialysis.

Inclusion criteria

  • English speaking
  • >18 yrs age
  • chronic kidney disease, documented GFR\<30ml/min by abbreviated MDRD calculation

Exclusion criteria

Exclusion Criteria:

  • Inpatients
  • Pediatric patients
  • Non-English speaking patients
  • established dialysis patients
  • patients receiving iodinated contrast within 30 days of current procedure
  • patients with central arterial manipulation within 30 days of current procedure
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
0 participants (actual)

Groups and cohorts

  • Observation

    Chronic kidney disease patients presenting for fisulta evaluation with documented GFR\<30ml/min by abbreviated MDRD calculation.

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What researchers measure

Primary outcomes

  1. Assess the impact of conventional dose iodinated contrast on the renal function of stage 4 and 5 chronic kidney disease patients undergoing arteriovenous fistula evaluation using a standard sodium bicarbonate prophylaxis protocol.

    Time frame: 48 hours

Secondary outcomes

  1. Assess the impact of conventional dose iodinated contrast on urinary kidney injury marker-1 (KIM-1) levels.

    Time frame: 3 hours and 48 hours

  2. Assess the impact of different patient characteristics on the development of contrast-induced kidney injury, such as diabetes, coronary artery disease, hypertension, and angiotensin converting enzyme inhibitor therapy.

    Time frame: Baseline patient charcteristics.

07

Study locations

1 site
  • Maine Medical Center - Brighton Campus
    Portland, Maine 04101, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 20, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00621972
Lead sponsor
MaineHealth
Responsible party
Sponsor
First posted
Feb 22, 2008
Start date
Jan 2008
Primary completion
Nov 2009
Completion
Nov 2009
Last update
Sep 20, 2018

Study contacts

Scott M Benson, D.O.
principal investigator · Maine Medical Center - Division of Nephrology

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Sep 2018. You cannot join it, but the record below documents what was studied.

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