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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

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

MedlinePlus related topics:   Dialysis    Kidney Failure   

U.S. FDA Resources

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


Study ID Numbers:   NCRR-M01RR00036-0781
First Received:   March 6, 2001
Last Updated:   June 23, 2005
ClinicalTrials.gov Identifier:   NCT00012441
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

ClinicalTrials.gov processed this record on October 10, 2008




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