|
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
![]() |
||||||||||||||||||||||||||||||||||||
| Sponsor: | 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 |
Eligibility| Ages Eligible for Study: | 21 Years to 75 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Adult patients with chronic renal failure requiring intermittent hemodialysis with a life expectancy of greater than 2 years
Contacts and 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. | |
More Information
| 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 |
|
Renal Dialysis |
|
Renal Insufficiency Urologic Diseases Renal Insufficiency, Chronic |
Kidney Failure, Chronic Kidney Diseases Kidney Failure |