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Blood Pressure Variability clinical trials

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NCT ID: NCT06012487 Not yet recruiting - Clinical trials for Blood Pressure Variability

Correlates and Control of Blood Pressure Variability

Start date: May 1, 2024
Phase: Phase 1
Study type: Interventional

The purpose the research is to prospectively demonstrate agreement between EHR and ambulatory blood pressure monitor (ABPM) derived blood pressure variability (BPV), as well as the feasibility of reducing BPV using a data-driven pharmacotherapeutic approach. To this end, this is a feasibility study that will make use of the Cedars-Sinai Health System including the Medical Delivery Network and the clinics of all practitioners who use the same EHR.

NCT ID: NCT05756257 Not yet recruiting - Clinical trials for Acute Ischemic Stroke

Blood Pressure Variability and Ischemic Stroke Outcome

BP-VISO
Start date: May 2024
Phase:
Study type: Observational

The goal of this observational study is to evaluate the role of blood pressure (BPV) variability in patients suffering from acute ischemic stroke. The main questions it aims to answer are: 1. To determine the association of BPV with functional/cognitive outcome after ischemic stroke. 2. To determine a pathophysiologic mechanism of BPV's deleterious effect on functional outcome. 3. To evaluate potential treatment targets to pharmacologically reduce BPV after ischemic stroke.

NCT ID: NCT05232240 Recruiting - Clinical trials for Ischemic Cerebrovascular Disease

Blood Pressure Variability in Non-hypertensive Patients With Ischemic Cerebrovascular Disease

BPV-NhICVD
Start date: February 14, 2022
Phase:
Study type: Observational

This study is a single-center prospective cohort of patients with ischemic cerebrovascular disease (ICVD) who have not met the diagnostic criteria for hypertension. Ambulatory 24-hour blood pressure monitoring (ABPM) will be performed at baseline and one year after the enrollment. The primary purpose of the study is to delineate the relationship of blood pressure variability (BPV) with the risk of composite vascular events in non-hypertensive patients with ICVD. The factors related to BPV, as well as the potential modulators of the associations between BPV and vascular risk, will be further explored among these patients.

NCT ID: NCT04342468 Completed - Hypertension Clinical Trials

Blood Pressure Variability and Cardiovascular Disease Events in Patients With Hypertension

BPV
Start date: July 14, 2017
Phase:
Study type: Observational

Cardiovascular Disease (CV) including stroke is the leading cause of death in Malaysia Hypertension is a major contributor to this. Prevalence of hypertension in Malaysia is high (42%) in adults age 30 years or older. Besides the actual blood pressure (BP) level recently, blood pressure variability (BPV) has been recognized as an independent and strong predictor of CV events especially strokes. However, data on the BP variability and its relationship to CV events is very limited in Asia, particularly in Malaysia. Hence the investigators aim to study BPV and its relationship to CV events in treated hypertensive patients

NCT ID: NCT04314557 Recruiting - Hypertension Clinical Trials

Renal Arterial Denervation in Sympathetic Dysautonomia

RANSOM
Start date: March 14, 2019
Phase:
Study type: Observational [Patient Registry]

The RANSOM registry is considered as a collection of data with the ultimate purpose of gathering information about the effect of renal denervation in patients of the investigator's center and evaluating the results within the usual clinical practice. The general objective of the study is to evaluate the clinical results (blood pressure, quality of life and levels of catecholamines) as well as safety of renal sympathetic denervation in hypertensive patients, at least in treatment with an antihypertensive drug and with increased variability, considering as such a standard deviation> 10 mmHg for systolic BP and> 5 for diastolic BP of its blood pressure levels, measured by ABPM.

NCT ID: NCT03207100 Completed - Clinical trials for Blood Pressure Variability

Analgesia-first Minimal Sedation for Spontaneous Intracerebral Hemorrhage Early Antihypertensive Treatment

ASSICHH
Start date: December 6, 2017
Phase: N/A
Study type: Interventional

This study evaluates safety and efficacy of analgesia-first minimal sedation as an early antihypertensive treatment for spontaneous intracerebral hemorrhage. The analgesia-first minimal sedation strategy relies on the remifentanil-mediated alleviation of pain-induced stress response and the antisympathetic activity of dexmedetomidine to restore the elevated blood pressure to normal level in patients with spontaneous intracerebral hemorrhage. This strategy allows rapid stabilization of blood pressure, and its use as a pre-treatment for patients on mechanical ventilation prior to painful procedures reduces blood pressure variability and thereby results in etiologic treatment. It is more effective in blood pressure control than conventional symptomatic antihypertensive treatment, reduces the incidence of early hematoma expansion and improves prognosis, ,lowers healthcare workers workload, increases patient adherence, and improves healthcare worker satisfaction.

NCT ID: NCT01665235 Recruiting - Clinical trials for Blood Pressure Variability

Blood Pressure Variability and the Prognosis of Ischemic Stroke With Intracranial Artery Stenosis

Start date: August 2012
Phase: N/A
Study type: Interventional

Correlation study about Blood Pressure Variability and the prognosis of ischemic stroke with intracranial artery stenosis

NCT ID: NCT00943774 Completed - Clinical trials for Heart Rate Variability

High Resolution Phenotyping in Healthy Humans

Start date: April 2006
Phase: N/A
Study type: Observational

Baroreflex sensitivity is integral to blood pressure regulation, and varies among healthy, normotensive individuals. A reduced compensatory ability of baroreflex buffering in patients with carotid denervation results in blood pressure variability and an elevated blood pressure response to mental stress. Furthermore, 24-hour ambulatory blood pressure variability may also be a significant and independent risk determinant of cardiovascular disease. It remains unknown whether the degree of baroreflex sensitivity and ambulatory blood pressure variability are predictive of the pressor response to sympathoexcitatory stress in healthy humans. In this study the investigators propose a comprehensive evaluation of the relationships among the pressor and forearm vasodilator response to sympathoexcitation, ambulatory blood pressure variability, and baroreflex sensitivity in healthy normotensive subjects. Ultimately this study will provide preliminary data and protocol development for large-scale high resolution phenotyping in population-based trials aimed at determining the functional relevance of candidate gene variation in intermediate physiological traits pertinent to the pathogenesis of hypertension and cardiovascular disease.