Clinical trials

3

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Protecting Renal Function in Chronic Kidney Disease Patients with Isolated Nighttime Hypertension

Hypertension guidelines recommend the application of ambulatory blood pressure monitoring in the diagnosis and treatment of patients with hypertension. Subtypes of hypertension such as nocturnal hypertension can be found through ambulatory blood pressure monitoring. Previous studies have reported that the prevalence of nocturnal hypertension, even isolated nocturnal hypertension, is higher in patients with chronic kidney disease, and it is associated with adverse events such as cardiovascular events and progression of renal dysfunction. However, the benefit of controlling nocturnal hypertension in patients with chronic kidney disease is unclear. In this study, a total of 200 patients with chronic kidney disease and isolated nocturnal hypertension will be enrolled. Patients will be randomly divided into two treatment groups: the active antihypertensive treatment group and the placebo treatment group (1:1). The antihypertensive treatment group will be treated with arotinolol or amlodipine and clonidine to control nocturnal blood pressure, while the control group will be treated with the corresponding placebos. Randomized patients will be followed up for 2 years to evaluate the effect of controlling isolated nocturnal hypertension on the progression of chronic kidney disease in terms of EPI-estimated glomerular filtration rate (eGFR) decline and change in proteinuria.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Shanghai Institute of HypertensionUpdated: Jan 17, 2025
Eligibility criteria

Participants must be 18 years of age or older. All genders are eligible; [+5]

Presence of acute kidney injury or acute renal failure; [+13]

Status: Recruiting

Registry Study on "Control Nocturnal Hypertension to Reach the Target "

Ambulatory blood pressure monitoring (ABPM) is a major innovation in the history of hypertension diagnosis. In clinical practice, the most well established indication for using ABPM is to identify patients who have high BP readings in the office but normal readings during usual daily activities outside of this setting or vice versa, and to identify varying 24-h BP profiles. However, in recent years, there has been increasing interest in BP values during sleep, and nocturnal BP is now recognized to be superior to daytime BP in predicting fatal and nonfatal cardiovascular events (stroke, myocardial infarction, and cardiovascular death), especially in medicated patients. The current direction in the management of hypertension is toward earlier and lower BP control for 24 hours, including the nocturnal and morning periods. Therefore, it may be of great significance to pay attention to the management of nocturnal blood pressure so as to reduce the increased cardiovascular risks. Information of nocturnal hypertensive patients defined by ABPM was prospectively registered nationwide, and then to investigate whether there was difference in cardiovascular prognosis according to the control of ambulatory nocturnal blood pressure.

Participants needed: 4,500
Trial details
Age: 50-79Biological sex: AllType: ObservationalSponsor: Shanghai Institute of HypertensionUpdated: Jan 6, 2025Locations: 1Duration: 3 Years
Eligibility criteria

Age 50-79 years old [+5]

Without antihypertensive drug use [+2]

Status: Recruiting

Home Blood Pressure Intervention in the Community Trial

The primary purpose of the study is to explore whether a lower home blood pressure target (125/75 v.s. 135/85 mmHg) would be beneficial to elderly treated hypertensive patients in terms of reduced incidence of cardiovascular events. The study also aims to promote the application of standardised and information-based home blood pressure monitoring in community hypertension management.

Participants needed: 10,000
Trial details
Age: 60-80Biological sex: AllType: InterventionalSponsor: Shanghai Institute of HypertensionUpdated: Jan 6, 2025Locations: 1
Eligibility criteria

Aged 60-80 years old [+3]

Arm circumference too large or too small (less than 18 cm or greater than 42 cm)... [+9]