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Sodium Thiosulfate Treatment of Vascular Calcification in ESRD
This study is currently recruiting participants.
Verified by Washington University School of Medicine, June 2008
Sponsors and Collaborators: Washington University School of Medicine
Barnes-Jewish Hospital Foundation
Genzyme
Information provided by: Washington University School of Medicine
ClinicalTrials.gov Identifier: NCT00568399
  Purpose

Cardiovascular disease is the major cause of death in the hemodialysis population and calcification of the major arteries (coronary, aorta, and carotid) are a play a central role in this process. The major causes of the calcification are many, including high levels of phosphorus, low levels of inhibitors of calcification, positive calcium balance, and oxidative stress. Once vascular calcification is present, it is usually progressive. There is no known treatment to reverse established vascular calcification.

Sodium thiosulfate has been used extensively and safely to treat calcific uremic arteriopathy (a disease, in part due to calcification of small arteries) in dialysis patients. It increases the solubility of calcium by up to 100,000 fold and is also a potent anti-oxidant. It therefore has to potential to also decrease the amount of calcium in large arteries in dialysis patients and, hence improve survival.

We will study hemodialysis (HD) patients at high risk for cardiovascular disease and death by obtaining a multigated CT (MDCT) Scan of the coronary arteries, carotid arteries and aorta and an assessment of coronary artery stenoses by a simultaneous intravenous infusion of contrast. At the same setting, we will perform tests of pulse wave velocity (PWV) and carotid ultrasound (CIMT)studies. In those patients at high risk for cardiovascular death, defined as a coronary artery calcification score (CACS)of greater than 50, sodium thiosulfate at a dose of 12.5-25 gm/1.73 M2 will be infused over 15-30 minutes after each dialysis treatment for 5 months. The above studies will then be repeated.


Condition Intervention
Hemodialysis
Cardiovascular Diseases
Drug: sodium thiosulfate

MedlinePlus related topics: Calcium Dialysis Dietary Sodium Kidney Failure
Drug Information available for: Sodium thiosulfate Sodium hyposulfite
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Open Label, Uncontrolled, Single Group Assignment, Efficacy Study
Official Title: The Effect of Sodium Thiosulfate Treatment on Vascular Calcification in End Stage Renal Failure Patients

Further study details as provided by Washington University School of Medicine:

Primary Outcome Measures:
  • A decrease in the coronary artery calcium score after 5 months of sodium thiosulfate treatment [ Time Frame: 5 months ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • An decrease in pulse wave velocity, thoracic aorta and carotid artery calcification and correlation between these findings and changes in coronary artery calcification scores. [ Time Frame: 5 months ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 52
Study Start Date: December 2007
Estimated Study Completion Date: December 2009
Estimated Primary Completion Date: December 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Treatment: Experimental
This is the only arm and involves active treatment with sodium thiosulfate in those subjects with high coronary artery calcium scores.
Drug: sodium thiosulfate
sodium thiosulfate 12.5-25 gm/M2 after each thrice weekly hemodialysis treatments for 5 months.

Detailed Description:

Hypothesis 1: The treatment of HD patients with high CAC scores with sodium thiosulfate for 5 months will decrease the amount of calcium in their coronary arteries.

Patients who are at high risk for having coronary calcification (history of MI, ischemic heart disease, peripheral or carotid artery disease) will be selected to undergo testing. We will recruit 52 HD patients receiving treatment in our units to undergo MDCT scanning along with non-invasive testing of PWV and CIMT. Assuming that 60% will have a CAC score of ≥50, 31 patients will be treated with sodium thiosulfate. We will administer 25% sodium thiosulfate solution (American Reagent Laboratories, Shirley, NY) at a dose of 12.5-25g/1.73m2 per over 15-30 minutes after each hemodialysis session for a total of 60 treatments (5 months). Assuming a 35% attrition rate, 20 patients will complete the entire protocol and undergo a repeat study of the initial battery of tests.

Rationale for treatment with sodium thiosulfate: Sodium thiosulfate, used as an antidote for cyanide poisoning for more than a century, is also an anti-oxidant, and binds with calcium to form a highly soluble calcium thiosulfate salt. The solubility of calcium thiosulfate salt is 250-100,000 fold higher than calcium oxalate or calcium phosphate salt. It has been used to treat recurrent calcium kidney stones and tumoral calcinosis (ectopic calcification usually around joints). It has also been used successfully in treating calcific uremic arteriopathy, a disease of small artery and soft tissue calcification, in several studies of dialysis patients and in our own experience of 5 patients. By 2 months there is radiological evidence of reduction in soft tissue calcification. Unpublished data also have demonstrated regression of established aortic calcification in uremic rats.

Sodium thiosulfate is a FDA approved medication for the treatment of cyanide poisoning. It is classified by the FDA as "generally recognized as safe". There are no known contraindications. The only side effects reported during intravenous (IV) administration in ESRD patients are nausea, vomiting and hyperosmia during the administration, which can be alleviated by pre-administration of anti-emetic medications. Sodium thiosulfate is slowly given through the dialysis venous line toward the end of HD treatments. The selected dose for this pilot study is the same as that used for the treatment of calcific uremic arteriopathy.

Hypothesis 2: Decreasing the CAC score will be associated with a decrease in the calcium content in other large arteries such as the thoracic aorta and carotid arteries.

Hypothesis 3: Decreasing the CAC score will be associated with a functional improvement of the vascular system (as assessed by pulse wave velocity).

Hypothesis 4: Decreasing the CAC score will be associated with a decrease in the severity of coronary artery stenoses.

Hypothesis 5: Decreasing the CAC will be associated with an increase in inhibitors of vascular calcification (such as fetuin-A) and/or decrease in promoters of vascular calcification (such as CRP).

We will freeze 10 ml of serum obtained prior to and then monthly during treatment for subsequent analyses. Included in the analysis will be Fetuin-A levels but other relevant markers will be considered. Blood will also be frozen for future genomic studies.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Hemodialysis patient with thrice weekly treatments
  • Coronary artery calcium score greater than 50
  • Age greater than 18
  • Compliant with hemodialysis treatments
  • Informed consent

Exclusion Criteria:

  • Allergy to sodium thiosulfate
  • Pregnancy
  • Incarceration
  • Enrollment in another study
  • Life expectancy less than 5 months
  • Expectation of recovery of renal function
  • Urine output of greater than 200 ml/day or contrast allergy will not receive intravenous contrast
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00568399

Contacts
Contact: James A Delmez, MD 314-362-7207 jdelmez@wustl.edu
Contact: Victor Davila, MD 314-362-4748 vdavila@im.wustl.edu

Locations
United States, Missouri
Washington University Recruiting
Saint Louis, Missouri, United States, 63110
Principal Investigator: James A Delmez, MD            
Sponsors and Collaborators
Washington University School of Medicine
Barnes-Jewish Hospital Foundation
Genzyme
Investigators
Principal Investigator: James A Delmez, MD Washington University School of Medicine
  More Information

Responsible Party: Washington University ( James Delmez )
Study ID Numbers: HRPO 07-0331
Study First Received: December 5, 2007
Last Updated: June 4, 2008
ClinicalTrials.gov Identifier: NCT00568399  
Health Authority: United States: Institutional Review Board

Keywords provided by Washington University School of Medicine:
Coronary
Calcification
Dialysis
Thiosulfate
Cardiovascular

Study placed in the following topic categories:
Sodium thiosulfate
Kidney Failure, Chronic
Kidney Failure

Additional relevant MeSH terms:
Anti-Infective Agents
Anti-Bacterial Agents
Antioxidants
Molecular Mechanisms of Pharmacological Action
Therapeutic Uses
Physiological Effects of Drugs
Cardiovascular Diseases
Chelating Agents
Antitubercular Agents
Protective Agents
Pharmacologic Actions
Antidotes

ClinicalTrials.gov processed this record on January 15, 2009