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Clinical Trial Details

Trial ID: L0005
Source ID: NCT02190318
Associated Drug: Losartan
Title: Residual Renal Function Preservation in Peritoneal Dialysis Patients
Acronym:
Status: UNKNOWN
Study Results: NO
Results:
Conditions: Chronic Renal Disease
Interventions: DRUG: Losartan|DRUG: spirolactone|OTHER: blank control
Outcome Measures: Primary: residual renal function of peritoneal dialysis patients, From date of randomization until the date of dropping out of the study or death from any cause, whichever came first, assessed up to 12 months. | Secondary: peritoneal membrane function, peritoneal membrane function is measured by peritoneal equilibration test to test the type of peritoneal transport. Briefly, a standard 4-hour dwell period was used (first exchange of the day), using a 2.5% glucose concentration 2-L volume exchange. The patient used their usual overnight dialysis regimen, and both the overnight and test drainage volumes were measured.The dialysate:plasma ratio of creatinine at the completion of the 4-hour dwell period (D/Pcreat) was used as the estimate of low-molecular-weight solute transport., From date of randomization until the date of dropping out of the study or death from any cause, whichever came first, assessed up to 12 months.
Sponsor/Collaborators: Sponsor: Second Xiangya Hospital of Central South University | Collaborators: Baxter Healthcare Corporation
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases:
Enrollment: 96
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2013-11
Completion Date: 2015-12
Results First Posted:
Last Update Posted: 2014-08-01
Locations: Changsha, Hunan, 410000, China
URL: https://clinicaltrials.gov/show/NCT02190318