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Comparison of Daily Nocturnal Hemodialysis With Daily Hemodialysis
This study is currently recruiting participants.
Verified by National Center for Research Resources (NCRR), December 2003
First Received: March 6, 2001   Last Updated: June 23, 2005   History of Changes
Sponsored by: National Center for Research Resources (NCRR)
Information provided by: National Center for Research Resources (NCRR)
ClinicalTrials.gov Identifier: NCT00012441
  Purpose

Hemodialysis remains associated with a high mortality (approximately 22% per year) and many complications despite improvements over the last twenty years. Several nephrologists have suggested that increasing the frequency and amount of dialysis will result in improved outcomes. In fact, various forms of daily dialysis have been performed in over 300 patients in the last 30 years with improvements in blood pressure, quality-of-life, bone disease, and other complications of renal failure. Whether this form of treatment can be expanded to the 220,000 Americans on hemodialysis is unknown. The primary outcome of this study is to determine the effectiveness of nocturnal dialysis in hemodialysis patients in St. Louis. If the pilot study is effective, then participation in a larger, multicenter trial is expected. The endpoints measured are use of antihypertensive medications, improvement in secondary hyperparathyroidism and use of phosphorus binders, quality-of-life measured by SF-36 surveys, and improvement in physical function as measured by maximal oxygen uptake.


Condition Intervention
Kidney Failure, Chronic
Procedure: hemodialysis

Study Type: Interventional
Study Design: Treatment, Non-Randomized, Efficacy Study
Official Title: Comparison of Daily Nocturnal Hemodialysis With Daily Hemodialysis

Resource links provided by NLM:

  Eligibility

Ages Eligible for Study:   21 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Adult patients with chronic renal failure requiring intermittent hemodialysis with a life expectancy of greater than 2 years

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00012441

Locations
United States, Missouri
Washington University School of Medicine Recruiting
St. Louis, Missouri, United States, 63108
Contact: Brent W. Miller, M.D.     314-286-0801        
Principal Investigator: Brent W. Miller, M.D.            
Sponsors and Collaborators
  More Information

No publications provided

Study ID Numbers: NCRR-M01RR00036-0781
Study First Received: March 6, 2001
Last Updated: June 23, 2005
ClinicalTrials.gov Identifier: NCT00012441     History of Changes
Health Authority: United States: Federal Government

Keywords provided by National Center for Research Resources (NCRR):
Renal Dialysis

Study placed in the following topic categories:
Renal Insufficiency
Urologic Diseases
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Kidney Diseases
Kidney Failure

Additional relevant MeSH terms:
Renal Insufficiency
Urologic Diseases
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Kidney Diseases
Kidney Failure

ClinicalTrials.gov processed this record on July 02, 2009