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Essential Hypertension clinical trials

View clinical trials related to Essential Hypertension.

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NCT ID: NCT04915313 Completed - Prehypertension Clinical Trials

The Antihypertensive Effect of Remote Ischemic Conditioning (RIC-HTN).

Start date: June 15, 2021
Phase: N/A
Study type: Interventional

This study intends to further reveal the antihypertensive effect of LRIC and explore its potential mechanisms.

NCT ID: NCT04830449 Completed - Hypertension Clinical Trials

Clinical Efficacy and Safety Evaluation of HCP1904-2 in Essential Hypertension Patients

Start date: October 29, 2020
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate of efficacy and safety of HCP1904-2 and RLD2001-2 alone in patients with essential hypertension inadequately controlled on RLD2001-2 monotherapy.

NCT ID: NCT04820907 Completed - Hypertension Clinical Trials

Clinical Efficacy and Safety Evaluation of HCP1904-1 in Essential Hypertension Patients

Start date: October 27, 2020
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate of efficacy and safety of HCP1904-1 and RLD2001-1 alone in patients with essential hypertension inadequately controlled on RLD2001-1 monotherapy.

NCT ID: NCT04521582 Completed - Clinical trials for Hypertension,Essential

Management of Hypertension Utilizing Trained Community Health Worker in Rural Municipalities of Nepal

MUTU
Start date: April 27, 2021
Phase: N/A
Study type: Interventional

The investigators will evaluate whether a system involving Female Community Health Volunteers (FCHVs) and facility-based community health workers (FB-CHWs) of Health Post (Auxiliary Health Workers, Auxiliary Nurse Midwives and Health Assistant) can contribute to improving hypertension care in rural Nepal. This study will be conducted in Rupa (active group) and Biruwa (comparison group) Rural Municipality of Gandaki province and enroll at least 736 hypertensive adults (322 in Rupa Rural Municipality and 414 in Biruwa Rural Municipality) who are aged 25-70 years, not taking antihypertensive medication, not pregnant and not breastfeeding, free of prior cardiovascular disease, chronic kidney disease, and diabetes. In Rupa Municipality, eligible participants will be able to receive amlodipine, one of the most frequently used antihypertensive medications, from FB-CHWs at Health Posts and five times (including baseline and end of study) of lifestyle counseling by FCHVs, whereas participants in Biruwa Municipality will receive the usual care plus three times (including baseline and end of study) of lifestyle counseling by FCHVs.

NCT ID: NCT04495231 Completed - Clinical trials for Diabetes Mellitus, Type 2

Sympathetic Activity and Cardiometabolic Complications

SYMPACT
Start date: September 1, 2007
Phase:
Study type: Observational

Recent studies on catecholamine physiology have shown a direct correlation with arterial hypertension, overcoming the exclusive role in the diagnosis and follow-up of chromaffin tumors. Nevertheless, in literature, few studies explore and reveal the utility of testing metanephrines for the evaluation of sympathetic activity and its associated cardiometabolic complications in patients with essential hypertension.

NCT ID: NCT04488978 Completed - Clinical trials for Essential Hypertension

Phase 2 Study to Evaluate the Efficacy and Safety of Irbesartan and Amlodipine Combined or Alone in Patients With Essential Hypetension

Start date: May 21, 2020
Phase: Phase 2
Study type: Interventional

A Randomized, Double-blind, Multicenter, Factorial Design, Phase II Study to Evaluate the Efficacy and Safety of Irbesartan and Amlodipine Combined or Alone in Patients With Essential Hypertension

NCT ID: NCT04470830 Completed - Clinical trials for Essential Hypertension

A Study for PMS of AZL-M/CLD FDC in the Treatment of Participants With Essential HTN in South Korea

Start date: September 11, 2019
Phase:
Study type: Observational

The purpose of this study is to evaluate the safety by assessing all serious and non-serious adverse events (AEs), irrespective of relatedness or expectedness, as well as other safety parameters including laboratory values, serious adverse events (SAEs)/serious adverse drug reactions (ADRs), unexpected AEs and ADRs that are not reflected on the precaution in the use, ADRs already known, non-serious ADRs and other safety related information (laboratory values changes, etc).

NCT ID: NCT04470817 Completed - Clinical trials for Essential Hypertension

A Study for PMS of AZL-M in the Treatment of Adult Participants With Essential Hypertension in South Korea

Start date: August 7, 2018
Phase:
Study type: Observational

The purpose of this study is to evaluate the safety by determining the incidence rates of all adverse events (AEs) including serious adverse events (SAEs)/serious adverse drug reactions (ADRs), unexpected AEs and ADRs that are not reflected on the precaution in the use, ADRs already known, non-serious ADRs and other safety related information (laboratory values changes, etc).

NCT ID: NCT04459741 Completed - HIV-1-infection Clinical Trials

HIV, Immune Activation and Salt Sensitive Hypertension

HISH
Start date: January 2, 2019
Phase: N/A
Study type: Interventional

High dietary salt is associated with immune activation, elevated levels of inflammatory cytokines and hypertension in murine models. Hypertension is independently associated with inflammation in both murine studies and studies in humans. In people living with HIV, these interactions are not well established. The aim of this study is to determine the effect of excess dietary salt on immune cell activation, pro- and anti-inflammatory cytokines and blood pressure between individuals with and without hypertension among people living with HIV and HIV negative persons.

NCT ID: NCT04303689 Completed - Clinical trials for Essential Hypertension

Repurposing Colchicine to Improve Vascular Function in Hypertension

RECTIFHY
Start date: August 1, 2020
Phase: N/A
Study type: Interventional

In this project the potential beneficial effect of the drug colchicine on vascular reactivity and blood pressure will be assessed. Colchicine is a commonly used anti-inflammatory medication approved for the treatment of gout, Familial Mediterranean Fever and pericarditis in Denmark. The current project idea is based on accumulating evidence in the literature for a beneficial role of colchicine treatment in the prevention of cardiovascular disease in parallel with novel mechanistic insight from our own research. Recently, colchicine was associated with a lower risk of cardiovascular disease, including reduced myocardial infarctions, strokes and acute coronary syndrome . However, none of these trials have investigated the effect of colchicine on arterial tone or stiffness, changes to which may underlie the reduced risk of cardiovascular disease associated with colchicine. In support of the hypothesis that colchicine will improve vascular reactivity, a study in 1985 by Lagrue et al. found that daily, low-dose colchicine improved arterial stiffness in a small cohort of hypertensive patients. More recently, colchicine was shown to improve arterial stiffness in patients with Familial Mediterranean fever supporting a cardiovascular protective role of colchicine. Finally, colchicine is also proposed to have anti-inflammatory effects in the vascular system.