Effect of N-Acetylcysteine on Residual Renal Function in Chronic Hemodialysis Patients
Recruitment status was Not yet recruiting
| Tracking Information | |||||
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| First Received Date ICMJE | July 24, 2007 | ||||
| Last Updated Date | July 24, 2007 | ||||
| Start Date ICMJE | Not Provided | ||||
| Primary Completion Date | Not Provided | ||||
| Current Primary Outcome Measures ICMJE | Not Provided | ||||
| Original Primary Outcome Measures ICMJE | Not Provided | ||||
| Change History | No Changes Posted | ||||
| Current Secondary Outcome Measures ICMJE | Not Provided | ||||
| Original Secondary Outcome Measures ICMJE | Not Provided | ||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Effect of N-Acetylcysteine on Residual Renal Function in Chronic Hemodialysis Patients | ||||
| Official Title ICMJE | Not Provided | ||||
| Brief Summary | In our opinion, it is worth to check an ability of antioxidant therapy to produce a favorable effect on Residual Renal Function. The aim of our study is to investigate the effect of N-acetylsysteine on RRF in prevalent HD patients. |
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| Detailed Description | Background Preserving residual renal function (RRF) has always been the primary clinical goal for every nephrologists managing patients with chronic kidney disease but not yet on dialysis. RRF in patients on dialysis has proven to be a consistent and powerful predictor of mortality. This is particularly evident for patients treated with peritoneal dialysis (PD): CANUSA study showed that only RRF but not dialysis dose has significant predictive power of mortality [1]. Interestingly, there have been very few studies that have examined the contribution of RRF to outcome in hemodialysis (HD) patients. This is particularly unfortunate because HD patients counts more than 90% of all dialysis population both in Israel and USA. A single study showed that persistence of RRF significantly improved patients' outcome [2]. Moreover, it is well known that RRF deteriorates more rapidly in HD patients than in PD patients [3]. Preservation of RRF remains an unresolved problem in dialysis patients. The exact mechanism of rapid loss of RRF on HD is not fully understood. Several experimental and clinical studies showed that variety of vascular events and increased oxidative stress in dialysis patients may be due to inhibition of nitric oxide (NO) synthesis by ADMA (Asymmetric Dimethylarginine ), known to be endogenous inhibitor of NO synthetase [4]. ADMA may be significantly reduced by dialysis [5]. Metabolism of ADMA is primarily by the enzyme DDAH , which activity is decreased by inflammation, oxidative stress, diabetes mellitus and hypercholesterolemia [6]. Based on current knowledge, treatment aimed at reducing oxidative stress should decrease ADMA levels [6], and it is logical to suggest that such a therapy might help to preserve RRF in HD patients. In our opinion, it is worth to check an ability of antioxidant therapy to produce a favorable effect on RRF. One preliminary study on effect of antioxidant Vitamin E showed a small beneficial effect on ADMA in chronic kidney disease [7]. N-Acetylcysteine (NAC) is an active antioxidant proved to be safe and beneficial in hemodialysis patents [8]. In our recent study, NAC effectively reduced the ototoxic effect of gentamicin in chronic hemodialysis patients [9]. The aim of our study is to investigate the effect of N-acetylsysteine on RRF in prevalent HD patients. Methods. Study population. The study will include 20 patients with ESRD, treated with chronic hemo- dialysis in Assaf Harofeh Medical Center. Patients will be excluded from the study if they are:
After performance of baseline clinical and laboratory examination the patients will receive orally NAC 1200 mg x 2/day for 2 weeks. At the end of this therapy, a follow up PET and Kt/V examination will be performed. These baseline and follow up clinical and laboratory examination will be performed at outpatient basis in our dialysis unit. The clinical monitoring of all the patients will include: 1. Blood Pressure and Heart Rate - at each of two visits. 2. Review of current medications and doses. 3. Body weight - at each of two visits. 4. Dialysis adequacy: Kt/V 6. Residual renal function examination: 24 hours urinary collection for urea and creatinine and calculation of CCT and residual Kt/V both at baseline and follow up visits. 7. Biochemical studies: ADMA, DDAH, NO - both at baseline and follow up visits. Statistical analysis The statistical analysis will be performed using the statistical software SPSS-version 10. Parametric data will be expressed as means ± standard deviation and compared by the standard t-test. Non-parametric data will be compared using chi square test. p value of 0.05 or less will be considered significant. References
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| Study Type ICMJE | Interventional | ||||
| Study Phase | Not Provided | ||||
| Study Design ICMJE | Intervention Model: Single Group Assignment Masking: Open Label |
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| Condition ICMJE |
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| Intervention ICMJE | Drug: N-acetylcysteine | ||||
| Study Arm (s) | Not Provided | ||||
| Publications * | Not Provided | ||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Not yet recruiting | ||||
| Enrollment ICMJE | Not Provided | ||||
| Completion Date | Not Provided | ||||
| Primary Completion Date | Not Provided | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | 20 Years to 90 Years | ||||
| Accepts Healthy Volunteers | Not Provided | ||||
| Contacts ICMJE |
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| Location Countries ICMJE | Israel | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT00507052 | ||||
| Other Study ID Numbers ICMJE | 346147RRF | ||||
| Has Data Monitoring Committee | Not Provided | ||||
| Responsible Party | Not Provided | ||||
| Study Sponsor ICMJE | Assaf-Harofeh Medical Center | ||||
| Collaborators ICMJE | Not Provided | ||||
| Investigators ICMJE |
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| Information Provided By | Assaf-Harofeh Medical Center | ||||
| Verification Date | July 2007 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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