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Essential Hypertension clinical trials

View clinical trials related to Essential Hypertension.

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NCT ID: NCT05359068 Completed - Clinical trials for Essential Hypertension

Study to Evaluate the Efficacy and Safety of SPH3127 In Patients With Mild-moderate Essential Hypertension

Start date: June 10, 2021
Phase: Phase 3
Study type: Interventional

The primary aim of the study is to assess the antihypertensive efficacy of SPH3127 in patients with mild to moderate essential hypertension.

NCT ID: NCT05288400 Completed - Clinical trials for Essential Hypertension

Evaluation of the Clinical Efficacy and Safety of Amlodipine 5mg/ Bisoprolol Fumarate 5mg /Perindopril Arginine 5mg Fixed-dose Combination in Capsule and Free Monotherapy at the Same Dose in Patients With Uncontrolled Essential Hypertension.

Start date: May 14, 2018
Phase: Phase 3
Study type: Interventional

The purpose of this study was to evaluate the efficacy and the safety of a fixed-dose combination in capsule of Amlodipine 5mg/ Bisoprolol fumarate 5mg/ Perindopril arginine 5mg, and free monotherapy at the same dose in patients with uncontrolled essential hypertension.

NCT ID: NCT05257291 Active, not recruiting - Clinical trials for Essential Hypertension

Study MIPAE - Melatonin and Essential Arterial Hypertension

MIPAE
Start date: February 2, 2018
Phase: Phase 2
Study type: Interventional

Study MIPAE - Melatonin and essential arterial hypertension. Study with dietary supplement, prospective and monocentric (randomized control trial). 1 mg/day of melatonin has been administered for one year to a group of patients suffering from essential hypertension (from at least one year) and who are already on antihypertensive therapy. This group has been compared with as many hypertensive patients on antihypertensive therapy to whom melatonin has not been administered. Each of the participants have been evaluated at the beginning of the study and after one year considering: - systolic and diastolic blood pressure; - echocardiographic values (Vivid Q, GE Healthcare); - applanation tonometry (SphygmoCor, AtCor Medical); - peripheral arterial tonometry (EndoPAT-2000, Itamar); - melatonin levels and total circulating antioxidant capacity after peripheral venous blood sampling. The aim of the study was to evaluate the antioxidant and vasoprotective effects of melatonin, evaluating both plasma changes and directly studying the possibility of a real remodeling and improvement of cardiac structures.

NCT ID: NCT05199129 Completed - Hypertension Clinical Trials

Clinical Efficacy and Safety Evaluation of HCP1904-3 in Essential Hypertension Patients

Start date: November 17, 2021
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate of efficacy and safety of HCP1904-3 and RLD2001-1 alone in patients with essential hypertension inadequately controlled on RLD2001-1 monotherapy.

NCT ID: NCT05185297 Completed - Hypertension Clinical Trials

Recreational Futsal for Controlled Hypertension

HyperFut
Start date: November 17, 2021
Phase: N/A
Study type: Interventional

Arterial hypertension (HT) was the leading global contributor for premature deaths in 2015. Its treatment includes medication and lifestyle changes, namely diet and regular exercise, which has shown to have an inverse relationship with arterial HT. Recreational soccer (RS) has proven to be a non-pharmacological treatment for several chronic conditions, including arterial HT, with meaningful decreases on blood pressure (BP). Recreation futsal (RF) is expected to elicit comparable BP changes to RS considering that it imposes similar physical and physiological demands. However, the effects of RF on BP and other cardiovascular markers have not been previously investigated in participants only with controlled arterial HT. Furthermore, acute BP changes and double product elicited by this exercise modality were never described. Therefore, the main purpose of this study is to assess if RF is an effective coadjuvant intervention for BP control in adults with controlled arterial HT. Secondary purposes are: i) to determine the impact of RF on other cardiovascular markers; ii) to describe the acute BP changes and the double product elicited by RF; and iii) to assess the impact of 1 month of detraining on BP and other cardiovascular markers (4 months).

NCT ID: NCT05165823 Completed - Clinical trials for Hypertension,Essential

The Significance of Sodium Balance and the Value of Salt-blood Test in Identifying Salt Sensitive Patients

VASA
Start date: February 8, 2022
Phase: N/A
Study type: Interventional

This is a randomized controlled trial with 72 patients with hypertension examining the effects on blood pressure of sodium restriction and whether the blood analysis Salt-blood test is associated to a decrease in blood pressure. Patients will be randomized 2:1 to either sodium restriction or usual diet for 4 weeks. Baseline measures will be done before intervention and outcome measures after the 4 weeks.

NCT ID: NCT05110898 Not yet recruiting - Hypertension Clinical Trials

Efficacy and Safety Study of the Fixed-dose Combination of Olmesartan + Indapamide When Compared to the Isolated Drugs in the Treatment of Hypertension.

OLINDA
Start date: August 1, 2022
Phase: Phase 3
Study type: Interventional

Phase III clinical trial, multicenter of non-inferiority, randomized, single-blind evaluation of fixed-dose combination of olmesartan + indapamide compared to the isolated drugs in the treatment of hypertension.

NCT ID: NCT05109013 Recruiting - Clinical trials for Essential Hypertension

Juvenile Essential Arterial Hypertension and Vascular Function

Start date: September 1, 2021
Phase:
Study type: Observational

The main goal of this study is to investigate the association of the juvenile essential arterial hypertension with systemic micro- and macrovascular reactivity and cerebral vascular function, and to examine the potential impact of elevated oxidative stress on this associations.

NCT ID: NCT05103813 Recruiting - Clinical trials for Essential Hypertension

Protective Effect of Beraprost Sodium Tablets on Reperfusion Therapy for Acute STEMI

Start date: May 1, 2022
Phase: Early Phase 1
Study type: Interventional

Protective effect of Beraprost Sodium Tablets on coronary microcirculation function and ventricular remodeling after reperfusion therapy for acute ST segment elevation myocardial infarction

NCT ID: NCT05095350 Completed - Hypertension Clinical Trials

Effect of Probiotics on Primary Hypertension

Start date: December 5, 2021
Phase: Early Phase 1
Study type: Interventional

Gut microbiota was found to play a causal role in the pathogenesis of hypertension. Probiotics were shown to have a potential anti-hypertensive effect in human/rodent studies. This study aims to explore the effect, safety, and underlying mechanisms of the combination of probiotics, containing 10 strains from Lactobacillus and Bifidobacterium, on hypertension, compared with placebo.