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Hypertension clinical trials

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NCT ID: NCT04565990 Completed - Clinical trials for Hypertension, Pulmonary

A Study of Selexipag in Participants Who Participated in a Previous Selexipag Study

SOMBRERO
Start date: May 3, 2021
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the long-term safety of selexipag while providing continued selexipag treatment for participants who were previously enrolled in an Actelion-sponsored study with selexipag and who derived benefit from selexipag in indications for which a positive benefit-risk has been established.

NCT ID: NCT04564118 Completed - Atrial Fibrillation Clinical Trials

A Retrospective Analysis of the Adherence to Clinical Practice Guidelines Using the "MedicBK" Digital Platform in Patients With Hypertension and Atrial Fibrillation

INTELLECT
Start date: September 1, 2020
Phase:
Study type: Observational

The Clinical Decision Support Systems (CDSS) based on real clinical data and its own algorithms can help to make the right choice. This trial is designed to assess the difference between retrospective electronic medical cards (EMC) therapy prescriptions and MedicBK prescriptions based on key patient characteristics.

NCT ID: NCT04559074 Completed - Hypertension Clinical Trials

Personalised Electronic Record Supported Optimisation When Alone for Patients With Hypertension

PERSONALCovdBP
Start date: October 23, 2020
Phase: Phase 4
Study type: Interventional

This trial is focusing on blood pressure control for patients with high blood pressure (hypertension) during the COVID-19 pandemic when seeing a doctor for advice may be difficult. The study utilises remote consultations by telephone or video conferencing. Patients record blood pressure and data into an electronic diary on their phone which is reviewed in consultations every 2 weeks by a clinician. Medication for this trial is amlodipine as an oral solution which is uptitrated accordingly for patients receiving medication (anticipated 200). 800 patients will be in an observational group recording the same readings and will not receive any medication.

NCT ID: NCT04554953 Completed - Clinical trials for Hypertension and Dyslipidemia

A Combination Drug Including Fimasartan and Statins in Patients With Hypertension and Dyslipidemia

FIMASTAR
Start date: April 13, 2020
Phase:
Study type: Observational

The primary objective of this study is to evaluate the effectiveness of a combination drug containing fimasartan and statins on the control of hypertension and dyslipidemia, and the secondary objective is to evaluate the drug cost reduction effect, patients' satisfaction level and safety of the combination drug administration.

NCT ID: NCT04554810 Completed - Hypertension Clinical Trials

Pharmacists Improving Refugees' Adherence and Knowledge of Their Chronic Medications

Start date: May 10, 2015
Phase: N/A
Study type: Interventional

This study is a randomized, controlled, single-blinded clinical study which conducted over six months (May to October 2016) in different Jordanian cities, where most of Syrian refugees reside. The primary aim of this study was to assess refugees' adherence and knowledge of their chronic medications, and impact of the medication management review (MMR) service delivered by a clinical pharmacist on their adherence and knowledge of their chronic medications three months following delivering the service. An informed consent form was signed by all participants who accepted to participate (n=106). Participants were then randomized into intervention and control groups. The first group would have received the medication management review service during the study period, while the to the other group directly after the study was completed (after three months' time). Two validated questionnaire were used in the study for assessment; adherence to medications questionnaire and Knowledge about chronic medications questionnaire. These questionnaire were filled by tha patients at baseline and follow up home visits.

NCT ID: NCT04554147 Completed - High Blood Pressure Clinical Trials

Use of an Innovative Mobile Health Intervention to Improve Hypertension Among African-Americans

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

The project objective is to test the feasibility of delivering health education and self-management support to African-American patients with uncontrolled hypertension (HTN) through a culturally-tailored smartphone application (app)-enhanced intervention within federally qualified health centers.

NCT ID: NCT04554017 Completed - Hypertension Clinical Trials

Knowledge on Preventive Measures of Hypertension

Start date: March 15, 2020
Phase: N/A
Study type: Interventional

Hypertension among children and adolescents is on the rise in both developed and developing countries. Childhood and adolescent obesity, a key factor for hypertension in this population results largely from unhealthy dietary and physical inactivity behaviours. Adequate knowledge, a component for behavior change, has been found to be crucial to improving one's confidence to tackle these improper behaviours. Despite this, there are gaps in knowledge on hypertension and its risks factors in Ghanaian adolescents. Using an educational intervention (health talk), the study therefore sought to improve knowledge on preventive measures of hypertension among senior high school students in Ghana.

NCT ID: NCT04553653 Completed - Hypertension Clinical Trials

Improving Acute Hypertension Management Through Emergency Department Checklist

Start date: June 15, 2019
Phase: N/A
Study type: Interventional

The investigators hypothesize that the implementation of a checklist in acute severe hypertension would result in improving short and long-term outcomes of patients with acute severe hypertension treated in the emergency department (ED). The investigators hypothesize that in the short-term, a checklist would improve the diagnosis and management of end-organ damage as well as reduce the length of stay of acute severe hypertensive patients in the ED. The investigators hypothesize that the checklist will result in better compliance with anti-hypertensive medications than without the checklist at six-month post-discharge.

NCT ID: NCT04548986 Completed - Hypertension Clinical Trials

Single-center Prospective Study to Validate the Performance of the Aktiia Optical Blood Pressure Monitoring (OBPM) Device at the Wrist Against Ambulatory Blood Pressure Monitoring (ABPM)

OBPM_ABPM2020
Start date: August 6, 2020
Phase: N/A
Study type: Interventional

This study aims to assess the performances of optical blood pressure monitoring device, Aktiia.product in the context of cardiac rehabilitation program.

NCT ID: NCT04546308 Completed - Hypertension Clinical Trials

Central Arterial Hemodynamics and Resistance Training

Start date: December 21, 2019
Phase: N/A
Study type: Interventional

Resistance exercise training is one of the popular exercise modes that has been drawn the public's attention. However, existing evidence showed high-intensity resistance exercise training-induced negative adaptation on vascular function and blood pressure responses. Upper-body resistance exercise training is more likely to induced arterial stiffening, which has been shown to be gender-dependent. It is still unknown whether age also plays a role. We like to test the hypothesis that high-intensity upper body resistance exercise may lead to a higher increase of arterial stiffness, central blood pressure, and hemodynamic parameters in younger adults than older adults. We also hypothesize high intensity resistance training could contribute to greater central hemodynamic responses and muscle stiffness than the control; the change of muscle stiffness correlates with the change of hemodynamic parameters. Collectively, study 1 in this project is aimed to recruit 40 apparently healthy young (20-35yrs) and middle-aged to older adults (50-75yrs) into this study followed by upper-body or lower-body high-intensity exercise (80% 1 repetition maximum, 10 reps, 4 sets) by a randomized order. Blood draw, central blood pressure, hemodynamics will be performed and obtained at pre-, immediately-post, 20min, 40mins, and 60 mins post-exercise. Study 2 is aimed to investigate the effects of 8-week whole-body resistance exercise training followed by a 4-week detraining on above-measured variables in order to determine the long-term effects on resistance training. We will employee state-of-art ultrafast ultrasound to obtain muscle stiffness and carotid local pulse wave velocity. Endothelin-1 and catecholamines will also be measured to discover its underlying mechanisms on such stiffening effects induced by high-intensity resistance exercise.