Nighttime Losartan in Continous Ambulatory Peritoneal Dialysis (NVCAPD)
NCT03692013 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 68
Last updated 2018-11-05
Summary
Hypertension is one of the most important independent risk factors for the prognosis of continous ambulatory peritoneal dialysis patients. The incident rate is high and the control rate is low. Nocturnal hypertension has been paid more attention in recent years. Compared to daytime blood pressure, nocturnal blood pressure is an independent and efficient prognostic indicator of hypertensive deaths and cardiovascular events, but it is lack of evidence about its impact on prognosis in peritoneal dialysis patients and the effective treatment program. Our previous cohort study suggests that the incidence of nocturnal hypertension in patients with chronic kidney disease is up to 71.22%, with a significant increase as the decline of renal function, and more severe target organ damage in patients with nocturnal hypertension: the decrease of glomerular filtration rate, left ventricular hypertrophy, and the increase of all cause death and cardiovascular death. Our small sample size study show that night time antihypertensive drugs can better control blood pressure and delay the development of left ventricular hypertrophy. These preliminary results suggest that nocturnal hypertension is closely related to the prognosis of chronic renal disease. Taking antihypertensive drugs at night is one of the options for controlling nocturnal hypertension. However, it is not clear whether taking antihypertensive drugs at night can improve the prognosis of maintenance peritoneal dialysis patients with nocturnal hypertension. To this end, the investigators collect continous ambulatory peritoneal dialysis patients with nocturnal hypertension, and propose a time selective use of losartan to intervene in nocturnal hypertension. By comparing the difference in the effects of losartan on the prognosis of maintenance peritoneal dialysis patients during the day or night, to further clarify the role of nocturnal hypertension in the prognosis of maintenance peritoneal dialysis patients, whether controlling nocturnal hypertension can improve the prognosis of maintenance peritoneal dialysis patients. The completion of study will optimize the prevention and treatment of hypertension in maintenance peritoneal dialysis patients, and provide an evidence for precise prevention and treatment of nocturnal hypertension in maintenance peritoneal dialysis patients.
Conditions
- Hypertension,Nephropathy
Interventions
- DRUG
-
Losartan
Participants will be divided into 2 groups as daytime group and nighttime group The participants in daytime group will take 100-200mg Losartan in the morning between 6AM to 8AM. The participants in nighttime group will take 100-200mg Losartan at night between 9PM to 11PM .
Sponsors & Collaborators
-
Third Affiliated Hospital, Sun Yat-Sen University
collaborator OTHER -
Fifth Affiliated Hospital, Sun Yat-Sen University
lead OTHER
Principal Investigators
-
Cheng Wang, Director · Nephrology Department, the Fifth Affiliated Hospital of Sun Yat-Sen University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-12-01
- Primary Completion
- 2023-06-01
- Completion
- 2023-12-01
More Related Trials
-
Specific Blockage of Angiotensine 2 and Podocyturia in Glomerular Nephropathies With Hypertension and Proteinuria
NCT00369538 ·Status: SUSPENDED ·Phase: PHASE4
-
Attenuation of Cardiac Effects of Arteriovenous Fistula Creation With Losartan
NCT00602004 ·Status: COMPLETED ·Phase: NA
-
Hypertension in Hemodialysis Patients (Aim 3)
NCT00582114 ·Status: TERMINATED ·Phase: PHASE3
-
Add-on Pentoxifylline to Losartan Versus Increasing Dose of Losartan on NT-PRO BNP in Type 2 Diabetics With Nephropathy
NCT03006952 ·Status: COMPLETED ·Phase: PHASE4
-
Long-Term Renoprotection of Optimal Antiproteinuric Doses of Benazepril and Losartan in Chronic Renal Insufficiency
NCT00338091 ·Status: TERMINATED ·Phase: NA
-
Safety of Dual Blockage of Rennin-angiotensin System in Patients With Advanced Renal Insufficiency
NCT00630708 ·Status: TERMINATED ·Phase: NA
-
Removal of Beta Blocker Drugs by Hemodialysis
NCT03361280 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Efficacy of Candesartan on Brain Natriuretic Peptide Levels in Subjects With Chronic Heart Failure
NCT00843154 ·Status: TERMINATED ·Phase: PHASE3
-
Study of the Effect of Intradialytic Vasopressin on Chronic Hypertension in Patients With End Stage Renal Disease
NCT01247090 ·Status: COMPLETED ·Phase: PHASE2
-
Aldosterone Blockade in Chronic Kidney Disease: Influence on Arterial Stiffness and Kidney Function
NCT01100203 ·Status: TERMINATED ·Phase: PHASE3
-
Indapamide Versus Hydrochlorothiazide in Elderly Hypertensive Patients With Renal Insufficiency
NCT01172431 ·Status: COMPLETED ·Phase: PHASE4
-
Proof-of-concept for the Aldosterone Synthase Inhibitor LCI699 in Patients With Primary Hyperaldosteronism
NCT00732771 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy of Candesartan on Symptomatic Heart Failure in Treating Diabetic and Hypertensive Patients.
NCT00775840 ·Status: COMPLETED ·Phase: PHASE3
-
Effect of Add-on Spironolactone to Losartan Versus Losartan Alone on Peritoneal Membrane Among Peritoneal Dialysis Patients
NCT03953950 ·Status: UNKNOWN ·Phase: PHASE4
-
Azilsartan in Patients With Diabetic Kidney Disease and Hypertension
NCT05753696 ·Status: UNKNOWN ·Phase: NA
-
Comparison of the Role of Losartan Alone vs Hydrochlorothiazide Plus Losartan
NCT06491940 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Timing of Antihypertensive Medications on Key Outcomes in Hemodialysis
NCT03327909 ·Status: COMPLETED ·Phase: NA
-
Diurnal Variation of Plasminogen Activator Inhibitor-1
NCT00515021 ·Status: COMPLETED ·Phase: PHASE4
-
Bosentan Use in Patients With Diabetic Nephropathy
NCT00638131 ·Status: TERMINATED ·Phase: PHASE3
-
The Home Blood Pressure (BP) Trial
NCT05159999 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Long Term Tapering or Standard Steroids for Nephrotic Syndrome
NCT00308321 ·Status: UNKNOWN ·Phase: PHASE4
-
Improving Outcomes in Patients With Kidney Disease Due to Diabetes
NCT00381134 ·Status: COMPLETED ·Phase: PHASE2
-
The Effects of Lowering Dialysate Sodium in Hypertensive Hemodialysis Patients
NCT01455974 ·Status: COMPLETED ·Phase: NA
-
Anti-Proteinuric Response to ACEI, ARB and Diuretics Combination.
NCT00200694 ·Status: TERMINATED ·Phase: PHASE4
-
Night Time Use of Thiazide Diuretics for Improved Reduction in Stone Risk in Stone Formers With Elevated Urine Calcium
NCT02711670 ·Status: COMPLETED ·Phase: NA