Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Hypertension from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 19
- Active, not recruiting: 11
- Completed: 10
- Other: 10
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00081523 — Natural History of Sickle Cell Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 3500 |
| Study Type | OBSERVATIONAL |
| Conditions | Pain Crisis |
This study is not a treatment protocol and no experimental treatments are involved. Study participants may be seen as needed for clinical, translational and basic research studies, or as medically indicated. Subjects will receive their general medical care outside the NIH and will be seen at our clinic or at CNHS with varying frequency. Subjects may be seen for multiple visits. Subjects may be …
NCT01712620 — Spironolactone for Pulmonary Arterial Hypertension
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Institutes of Health Clinical Center (CC) |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary Arterial Hypertension |
| Interventions | ; |
Background:
- High blood pressure in the lungs, known as pulmonary arterial hypertension (PAH), is a rare disorder. In spite of recent advances in treatment, the death rate remains unacceptably high. Lung blood vessel function can be harmed by progressive injuries, such as inflammation, leading to worsening of the disease. A drug called spironolactone has been known to improve blood vessel fu…
NCT04154332 — Exosome Cargo From Preeclampsia Patients
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 64 |
| Study Type | OBSERVATIONAL |
| Conditions | Preeclampsia |
| Interventions |
Although extensively studied, the cause of preeclampsia remains uncertain other than it is thought that the placenta plays a critical role in the development of preeclampsia. Recent data revealed that exosomes released from the placenta could cause preeclampsia by transporting specific cargo responsible for the pathophysiological changes associated with the systemic disease. By isolating these …
NCT07218029 — A Clinical Study of Sotatercept (MK-7962) in People With Pulmonary Arterial Hypertension (MK-7962-038)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Merck Sharp & Dohme LLC |
| Enrollment | 815 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary Arterial Hypertension |
| Interventions |
Researchers are looking for more ways to treat PAH. In PAH, the blood vessels in the lungs become thick and narrow, which makes it harder for blood to flow. This causes high blood pressure in the lungs and overworks the heart. PAH can make it hard to breathe and be active. Some standard (usual) treatments for PAH can treat symptoms of PAH but do not stop PAH from getting worse.
Sotatercept is …
NCT05330221 — Project 2: ACHIEVE- HF
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Henry Ford Health System |
| Enrollment | 364 |
| Study Type | INTERVENTIONAL |
| Conditions | Heart Failure; Hypertension |
| Interventions | ; |
This project is part of the ACHIEVE GREATER (Addressing Cardiometabolic Health In Populations Through Early PreVEntion in the GREAT LakEs Region) Center (IRB 100221MP2A), the purpose of which is to reduce cardiometabolic health disparities in two cities: Detroit, Michigan, and Cleveland, Ohio. The ACHIEVE GREATER Center involves four separate but related projects that aim to mitigate health dis…
NCT06033131 — PI4 - A Trial Assessing Metformin to Prolong Gestation in Preterm Preeclampsia
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Lina Bergman |
| Enrollment | 294 |
| Study Type | INTERVENTIONAL |
| Conditions | Preeclampsia |
| Interventions | ; |
Preterm preeclampsia is a severe condition for both the mother and the fetus. Currently, the only treatment available to stop disease progression is termination/delivery of the fetus and placenta. Therefore, preterm preeclampsia carries the highest rates of neonatal morbidity and mortality due to iatrogenic preterm birth. There is evidence suggesting metformin, a drug commonly used to treat dia…
NCT06402968 — Clevidipine for the Antihypertensive Treatment of Acute Intracerebral Hemorrhage
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Zeenat Qureshi Stroke Institute |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Intracerebral Hemorrhage; Stroke; Hypertension |
| Interventions | ; |
The aim is to compare the rate of hypertensive subjects with ICH who reach SBP target with stability within 60 minutes of enrollment, among patients treated with IV clevidipine with those treated with alternate IV antihypertensive regimen.
NCT06352619 — Third Enhanced Control of Hypertension and Thrombectomy Stroke Domain Within ACT-GLOBAL Adaptive Platform Trial
| Status | Recruiting |
| Phase | N/A |
| Sponsor | The George Institute |
| Enrollment | 2000 |
| Study Type | INTERVENTIONAL |
| Conditions | Ischemic Stroke, Acute |
| Interventions | ; ; |
Several clinical trials have produced variable conclusions regarding the effects of intensive blood pressure (BP) lowering in post-EVT acute ischaemic stroke (AIS) patients. Although two trials indicate harm from very intensive target-based treatment (SBP <130 mmHg), the others neutral effects in the SBP range 140-160 mmHg. The ENCHANTED3/MT domain of the ACT-GLOBAL platform trial aims to test…
NCT05979168 — Effectiveness and Adoption of the TelTex4BP Intervention Among Adults With Hypertension in Nepal
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Central Department of Public Health |
| Enrollment | 500 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension; Medication Adherence; Blood Pressure; Cardiovascular Diseases |
| Interventions |
Despite evidence of preventing cardiovascular disease (CVD) risk through lifestyle changes, many patients with hypertension (HTN) do not comply with this and suffer from CVD and other complications. A previous study using a structured lifestyle intervention program has reported a 14% decrease in the 10-year risk of developing CVD at one year among hypertensive and diabetes patients. Low and Mid…
NCT06642246 — Sleep Promotion and Pediatric Hypertension
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Children’s Hospital of Philadelphia |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Insufficient Sleep; Hypertension |
| Interventions |
Determine the effectiveness and feasibility of a mobile health sleep extension approach in the pediatric nephrology setting, to increase sleep duration and reduce systolic and diastolic blood pressure.
NCT07683585 — Comparative Effectiveness of Dual Antihypertensive Regimens in Patients After Percutaneous Coronary Intervention
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Medical Research Center for Therapy and Preventive Medicine |
| Enrollment | 207 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension; Coronary Arterial Disease; Percutaneous Coronary Intervention |
| Interventions | ; |
This prospective randomized open-label study aims to compare the effectiveness of two dual antihypertensive therapy regimens in patients with arterial hypertension and coronary artery disease after elective percutaneous coronary intervention (PCI) with coronary artery stenting.
Patients requiring dual antihypertensive therapy will be randomized to receive either an angiotensin receptor blocker…
NCT07688928 — Efficacy and Safety of Finerenone Compared to Spironolactone in Treatment of Primary Aldosteronism
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Bangladesh Medical University |
| Enrollment | 104 |
| Study Type | INTERVENTIONAL |
| Conditions | Primary Aldosteronism; Endocrine Hypertension |
| Interventions |
The goal of this study is to compare the efficacy and safety of finerenone versus spironolactone in the treatment of hypertension due to primary aldosteronism.
It will be a randomized, double-blind, active-controlled, parallel-group clinical trial conducted at the Endocrine Hypertension Clinic, Department of Endocrinology, BSMMU. A total of 104 adult patients with confirmed primary aldosteroni…
NCT07377383 — Cardiometabolic Adaptations to Concurrent Training: Effect of Effort Configuration on Postmenopausal Women
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Universidade da Coruña |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Postmenopausal; Hypertension |
| Interventions |
The main objectives of this project are to assess the effects of a 20-week concurrent training program on neuromuscular adaptations, body composition, cardiometabolic health, quality of life, mood state, physical self-perception, and menopause-related symptoms in physically active postmenopausal women, and to compare the adaptations resulting from different combinations of endurance and resista…
NCT07601308 — Impact of Online Medical Misinformation
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Alexandria University |
| Enrollment | 402 |
| Study Type | OBSERVATIONAL |
| Conditions | Medical Misinformation; Medication Adherence; Health-Seeking Behavior; Chronic Diseases; Diabetes (DM) |
| Interventions |
A cross-sectional analytical study was conducted among adult patients diagnosed with chronic diseases to assess the impact of online medical misinformation on medication adherence, treatment decision-making, and health care-seeking behavior.
NCT07428473 — A Study of STX-1150 in Participants With Elevated Low-Density Lipoprotein Cholesterol (LDL-C)
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Monash University |
| Enrollment | 64 |
| Study Type | INTERVENTIONAL |
| Conditions | Elevated LDL-C and High Cholesterol |
| Interventions |
STX-1150 is an investigational therapy designed to lower LDL-C by silencing a gene called PCSK9 in the liver. STX-1150 does not edit or permanently change the gene. STX-1150 comprises an mRNA and guide RNA (gRNA) delivered via lipid nanoparticles (LNP) for intravenous infusion. The mRNA produces a protein that switches off the PCSK9 gene expression without altering the DNA sequence. This proces…
NCT07687745 — Breathing for Two: Inspiratory Muscle Strength Training for Supporting Healthy Blood Pressure in Pregnancy
| Status | Recruiting |
| Phase | Early Phase 1 |
| Sponsor | University of Arizona |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension Disorders in Pregnancy; Blood Pressure Measurement in Pregnancy; Inspiratory Strength Training (IST); Pregnancy |
| Interventions | ; |
This is an interventional study that will test whether a breathing exercise called Inspiratory Muscle Strength Training (IMST) can safely and effectively lower blood pressure during late pregnancy. The goal is to see if a home-based breathing training can help prevent or reduce high blood pressure disorders in pregnancy. The main objectives are to make sure the training is safe and tolerable fo…
NCT07042386 — Implementation of a Beauty Salon-Based Strategy for Blood Pressure Management Among Women
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Johns Hopkins University |
| Enrollment | 144 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension |
| Interventions | ; |
CROWN is a two-arm, cluster-randomized pilot trial testing the feasibility and preliminary efficacy of a salon-based cardiovascular intervention - training stylists as Heart Health Stylists to conduct in-salon blood pressure screenings, home monitoring with telehealth support, community health-worker coaching, and pharmacist-led medication management - among Black and Hispanic women with hypert…
NCT07341763 — Brain Stimulation Effects on Orientation and Mobility Skills in Adults With Vision Impairment
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Waterloo |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Retinitis Pigmentosa (RP); Rod Cone Dystrophy; Visually Impaired Persons; Peripheral Visual Field Defect of Both Eyes; Low Vision, Both Eyes |
| Interventions | ; |
This pilot clinical trial evaluates whether non-invasive brain stimulation improves the orientation and mobility (O&M) skills of individuals with constricted visual fields in both eyes. The study is composed of three visits. The first visit is meant to confirm eligibility by performing a few clinical tests. Eligible participants will then complete two additional visits, one in which the partic…
NCT07214376 — A Randomized Placebo-procedure Controlled Trial of the Enhancor System (PULmonary Artery Denervation) to Evaluate Safety and Efficacy in Patients With Combined Pre- and Post-capillary Pulmonary Hypertension Associated With Left Heart Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Pulnovo Medical, Inc. |
| Enrollment | 750 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary Hypertension; Heart Failure With Reduced Ejection Fraction; Hypertension; Vascular Diseases; Cardiovascular Diseases |
| Interventions | ; |
The goal of this clinical study is to evaluate the safety and efficacy of percutaneous pulmonary artery denervation with the Multi-Pole Pulmonary Artery Radiofrequency Ablation Enhancor System in patients with combined pre- and post-capillary pulmonary hypertension (CpcPH) associated with left heart disease (LHD). This randomized control trial will compare the investigational device (The Enhanc…
Active, Not Recruiting
NCT05649748 — An Extension Study of Treprostinil Palmitil Inhalation Powder (TPIP) for Pulmonary Arterial Hypertension (PAH)
| Status | Active, not recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | Insmed Incorporated |
| Enrollment | 91 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary Arterial Hypertension |
| Interventions | ; |
The primary purpose of the study is to evaluate the safety and tolerability of the long-term use of TPIP in participants with PAH from studies INS1009-201 (NCT04791514), INS1009-202 (NCT05147805) and other lead-in studies of TPIP in participants with PAH.
NCT05968859 — A Study of Pulmonary Hypertension Peripheral Limitations
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Mayo Clinic |
| Enrollment | 45 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary Arterial Hypertension; Healthy |
| Interventions | ; |
The investigators are doing this research study to compare whole body aerobic training with isolated leg training (with weights) and its impact on effectiveness in symptoms and quality of life in patients with Pulmonary Arterial Hypertension (PAH).
NCT06094491 — Virtual Diabetes Group Visits Across Health Systems
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Chicago |
| Enrollment | 720 |
| Study Type | INTERVENTIONAL |
| Conditions | T2DM (Type 2 Diabetes Mellitus); Hypertension; Heart Disease Chronic; Stroke; Hyperlipidemias |
| Interventions |
The purpose of this project is to evaluate the effectiveness of a virtual diabetes group visits on patients with type 2 diabetes mellitus (T2DM).
NCT06288659 — aSAH Treatment Based on Intraventricular ICP Monitoring: A Prospective, Multicenter, Randomized and Controlled Trial
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Huashan Hospital |
| Enrollment | 372 |
| Study Type | INTERVENTIONAL |
| Conditions | Aneurysmal Subarachnoid Hemorrhage; Intacranial Hypertension |
| Interventions |
ASTIM is a multicenter, prospective, randomised, blinded end-point assessed trial, to investigate the efficacy and safety of treatment based on intracranial pressure monitoring in improving the prognosis of patients with aneurysmal subarachnoid hemorrhage.
NCT06616974 — A Study of TX000045 in Patients With Pulmonary Hypertension Secondary to Heart Failure With Preserved Ejection Fraction (the APEX Study)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Tectonic Therapeutic |
| Enrollment | 191 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary Hypertension; Heart Failure With Preserved Ejection Fraction |
| Interventions | ; ; |
TX000045-003 is a double-blind, randomized, parallel group, placebo-controlled, proof- of-concept (POC) study, evaluating 2 dose regimens of TX000045 over the course of a 24-week treatment period (the APEX study).
NCT06744335 — Prospective Observational Multicenter Study of Patients With AH and CKD Markers in Kazakhstan (PROGRESS-CKD)
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | AstraZeneca |
| Enrollment | 1283 |
| Study Type | OBSERVATIONAL |
| Conditions | Rate of CKD Diagnosis in Patients With AH and CKD Markers; Demographic and Clinical Characteristics for Those Patients; Routine Therapy Before and After the Diagnosis of CKD |
Multicenter, non-interventional PRospective Observational study with retrospective analysis to describe the rate of CKD diaGnosis in patients with aRtErial hypErtenSion and CKD markerS in Kazakhstan
NCT06948773 — A Study of the Helix Surgical System in Primary Open-Angle Glaucoma (POAG) and Cataract (HELIX)
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Sight Sciences, Inc. |
| Enrollment | 25 |
| Study Type | INTERVENTIONAL |
| Conditions | Primary Open Angle Glaucoma; Cataract |
| Interventions |
A study to assess the safety of the Helix Surgical System in cataract surgery and to gain early evidence of its effectiveness in lowering intraocular pressure (IOP) in subjects with mild to moderate primary open-angle glaucoma (POAG) and cataracts.
NCT06964191 — Evaluate Efficacy and Safety of PA5108 Ocular Implants in Primary Open Angle Glaucoma or Ocular Hypertension
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | PolyActiva Pty Ltd |
| Enrollment | 75 |
| Study Type | INTERVENTIONAL |
| Conditions | Glaucoma, Open-Angle; Ocular Hypertension |
| Interventions | ; ; |
The goal of this clinical trial is to determine the dose of PA5108 Ocular Implant that is effective and safe for the reduction of intraocular pressure in adult patients with open-angle glaucoma or ocular hypertension, compared to the standard treatment therapy.
NCT06964061 — Evaluate Efficacy, Safety, Tolerability and Biodegradation of PA5346 Ocular Implant in Patients With Open-Angle Glaucoma or Ocular Hypertension
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | PolyActiva Pty Ltd |
| Enrollment | 12 |
| Study Type | INTERVENTIONAL |
| Conditions | Open Angle Glaucoma (OAG); Ocular Hypertension (OH) |
| Interventions |
The goal of this clinical study is to learn how effective and safe is a single administration of PA5346 Ocular Implant for the reduction of intraocular pressure in adult patients with open-angle glaucoma or ocular hypertension. It will also assess how long it takes for PA5346 Ocular Implant to dissolve in the eye.
NCT07067632 — Mortality Outcome of Controlled Blood Pressure Participants
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | DejthidaNathaphong |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Valid MeSH Conditions; Hypertension (HTN) |
| Interventions |
Despite advances in antihypertensive therapy, some patients with well-controlled blood pressure still experience fatal outcomes. This paradox raises critical questions about the efficacy of blood pressure-targeted interventions and whether BP control alone ensures survival. This systematic review and meta-analysis aims to evaluate all-cause mortality and cardiovascular death among hypertensive …
NCT07690397 — Dorzolamide/Brimonidine/Timolol Impact on Ocular Surface, Glaucoma Progression & Chatbot Follow-up: GLAUCO-TECH
| Status | Active, not recruiting |
| Phase | Phase 4 |
| Sponsor | Tecnoquimicas |
| Enrollment | 140 |
| Study Type | INTERVENTIONAL |
| Conditions | Primary Open-Angle Glaucoma (POAG); Ocular Hypertension |
| Interventions | ; |
The primary objective of this study is to evaluate the ocular surface safety of an ophthalmic solution indicated for the management of glaucoma, containing the active ingredients dorzolamide, timolol, and brimonidine, in patients diagnosed with primary open-angle glaucoma. The most relevant questions to be answered by this study are:
In patients with ocular hypertension or open-angle glaucoma,…
Not Yet Recruiting
NCT07688265 — Effect of Obesity Phenotype on Intraabdominal Pressure and Bleeding in Major Lumbar Spinal Surgery
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Marmara University Pendik Training and Research Hospital |
| Enrollment | 90 |
| Study Type | OBSERVATIONAL |
| Conditions | Lumbar Spinal Stenosis; Lumbar Degenerative Disease; Obesity; Intraabdominal Hypertension; Intraoperative Blood Loss |
| Interventions | ; |
Obesity is prevalent among patients with lumbar degenerative disease and is a known risk factor for perioperative complications in spinal surgery. However, most existing evidence relies solely on body mass index (BMI) without distinguishing between central and peripheral obesity phenotypes. Central and peripheral fat distribution may have distinct biomechanical and hemodynamic consequences, par…
NCT07599579 — Mobile Health Program for Post-Preeclampsia Hypertension
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Pittsburgh |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension (HTN); Preeclampsia; Hypertensive Disorders of Pregnancy (HDP) |
| Interventions | ; ; |
Strategies targeted to optimize hypertension (HTN) control for midlife women after hypertensive disorders of pregnancy (HDP) have not been studied, despite evidence of a critical need. This proposal targets the 10-20 years postpartum as a key time when women have subclinical cardiovascular (CV) sequelae of uncontrolled HTN and are primed for CV prevention interventions. Before proceeding with l…
NCT07679191 — Topical Application of Sucralfate in Promoting Healing of Esophageal Ulcers After Esophageal Varices Ligation
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | National Cheng-Kung University Hospital |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Ulcer Healing |
| Interventions |
Patients with EV bleeding often suffered from hematemesis, Tarry stool, and blood loss. Standard treatment for bleeding esophageal varices includes hemodynamic stabilization, pharmacological control, and endoscopic intervention. For endoscopic intervention, endoscopic variceal ligation (EVL) is the first-line therapy with 95% initial hemostasis success rate. However, after variceal ligation, es…
NCT07613099 — Fibrotic Disease Activity in Cardiopulmonary Disorders Using 18F-Fibroblast Activation Protein Inhibitor (18F-FAPI-74) PET/CT Imaging
| Status | Not yet recruiting |
| Phase | Phase 3 |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 210 |
| Study Type | INTERVENTIONAL |
| Conditions | Allogeneic Stem Cell Transplantation; Lung Allograft Transplantation; Interstitial Lung Disease; Acute Lung Injury; Pulmonary Arterial Hypertension |
| Interventions | ; |
Background:
Injury or diseases of the heart and lung can sometimes cause scar tissue (fibrosis) to build up in those organs. Current imaging scans can see this scar tissue once it has formed, but researchers want to find a way to detect the fibrosis in its earliest stages, while there might still be time to prevent serious damage. A new tracer (a radioactive substance injected during imaging s…
NCT07544836 — Navigating Hypertension and Food Insecurity
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Hawaii |
| Enrollment | 250 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension (HTN); Food Insecurity |
| Interventions | ; |
This multi-site randomized controlled trial uses a community-based approach to evaluate a Food as Medicine program for Native Hawaiian and Pacific Islander (NHPI) adults in Hawaii who have high blood pressure and difficulty affording healthy food. The study has two main goals: (1) to implement a produce prescription program and see if adding personal support from Community Health Workers (CHW) …
NCT07687160 — SPIRO-First: A Pragmatic Primary Care-Embedded Pilot Trial of Renin-Guided First-Line Antihypertensive Therapy
| Status | Not yet recruiting |
| Phase | Phase 4 |
| Sponsor | Ottawa Hospital Research Institute |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Early-stage Hypertension and Suppressed Renin |
| Interventions | ; ; |
The goal of this clinical trial is to determine whether a renin-guided antihypertensive treatment strategy is feasible to implement in community primary care clinics and to explore whether spironolactone improves blood pressure control in adults with low-renin hypertension.
The main questions it aims to answer are:
Is it feasible to identify, recruit, randomize, and follow adults with low-ren…
NCT07364682 — Measuring Heart Health in Both Term, Preterm and Unwell Newborn Babies With an Advanced Ultrasound Method: Speckle Tracking Echocardiography
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Birmingham Women’s NHS Foundation Trust |
| Enrollment | 190 |
| Study Type | OBSERVATIONAL |
| Conditions | Premature Baby; Pulmonary Hypertension of Newborn; Hypoxic Ischaemic Encephalopathy (HIE); Congenital Diaphragmatic Hernia; Chronic Lung DIsease |
This study aims to improve how neonatologists check the heart function of newborn babies, especially those who are sick. While standard heart ultrasound scans are useful, a more advanced and sensitive technique called 2D speckle tracking echocardiography (STE) can detect subtle problems with how the heart muscle squeezes and relaxes. This may allow doctors to spot potential issues earlier.
Our…
NCT07686120 — A Phase IIIb Study to Investigate the Effect of Baxdrostat in Chinese Participants With Uncontrolled Hypertension.
| Status | Not yet recruiting |
| Phase | Phase 3 |
| Sponsor | AstraZeneca |
| Enrollment | 286 |
| Study Type | INTERVENTIONAL |
| Conditions | Uncontrolled Hypertension |
| Interventions | ; |
This is a Phase IIIb, multicentre, randomised, double-blind, placebo-controlled, parallel group study to evaluate the effect of baxdrostat 2mg versus placebo, administered QD orally, on the reduction of ambulatory 24-hour average SBP in participants with uHTN.
Consenting participants will be screened within 4 weeks and will subsequently enter a 4-week run-in period with placebo. Thereafter, pa…
NCT07679984 — Evaluating the Effects of a Mindfulness Intervention on Health Outcomes in Individuals With Hypertension
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Ohio State University |
| Enrollment | 140 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension; Essential (Primary) Hypertension |
| Interventions |
The purpose of this study is to evaluate the effectiveness of adding the Mindfulness in Motion (MIM) program to usual primary care for people with high blood pressure. MIM is a facilitated, 8-week online program that teaches simple ways to manage stress using mindfulness practices. The program also includes the use of a companion smartphone app throughout the 12-month study period. In this stud…
NCT07115199 — Remote Patient Monitoring for Chronic Hypertension During Pregnancy (REACH)
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Rutgers, The State University of New Jersey |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Hypertension in Pregnancy |
| Interventions |
We hypothesize that frequent remote monitoring of blood pressure and real-time antihypertensive medication titration will optimize pregnancy outcomes in a clinically meaningful and cost-effective manner compared to the current standard of care. Therefore, this pilot study, as part of the K12 training support, will evaluate the feasibility of a randomized clinical trial to treat mild chronic hyp…
Completed Trials
NCT05075902 — Effect of Aerobic Training on the Health Parameters of Postmenopausal Women With Multimorbidity
| Status | Completed |
| Phase | N/A |
| Sponsor | Federal University of Uberlandia |
| Enrollment | 41 |
| Study Type | INTERVENTIONAL |
| Conditions | Multimorbidity; Multiple Chronic Conditions; Hypertension; Dyslipidemias |
| Interventions |
People affected by multiple chronic diseases have a greater chance of hospitalization, longer hospital stays, worse general health, worse physical and mental function and lower functional capacity, with an average risk of 50% of functional decline with each additional condition. The frequency of multimorbidity is higher in older, inactive women, who live in urban areas in low- and middle-income…
NCT04315571 — Comparing Ascites Relief In Two Standard Treatments: Large Volume Paracentesis Vs. Early Tips Using Viatorr Controlled Expansion Stents
| Status | Completed |
| Phase | N/A |
| Sponsor | University of California, Los Angeles |
| Enrollment | 68 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension, Portal; Ascites |
| Interventions | ; |
For this study, the investigators will be collecting data based on patients’ random selection to two different approved standard of care treatments for ascites: Subjects will get randomized into either Group A: Large Volume Paracentesis (LVP) with albumin infusion, or Group B: an early transjugular intrahepatic portosystemic shunt (TIPS) procedure.
NCT04258332 — CARDIA-Salt Sensitivity of Blood Pressure (SSBP)
| Status | Completed |
| Phase | N/A |
| Sponsor | Vanderbilt University Medical Center |
| Enrollment | 281 |
| Study Type | INTERVENTIONAL |
| Conditions | Salt Sensitivity of Blood Pressure; Hypertension |
| Interventions | ; |
Salt sensitivity of blood pressure (SSBP) is defined as the change in blood pressure (BP) in relation to change in salt intake. An increase in BP from low- to high-salt diet is common and associated with an increased risk of cardiovascular morbidity and mortality, even among normotensive individuals. Yet, the pathophysiology of SSBP is not well understood. The prevailing paradigm is that abnorm…
NCT05393232 — Groceries for Black Residents of Boston to Stop Hypertension Among Adults With Treated Hypertension
| Status | Completed |
| Phase | N/A |
| Sponsor | Beth Israel Deaconess Medical Center |
| Enrollment | 176 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension |
| Interventions | ; |
GoFreshRx is a randomized trial, testing the effects of a home-delivered DASH-patterned grocery intervention on blood pressure in Black adults actively treated for hypertension, residing in Boston area urban food deserts.
NCT05565716 — Supporting Self-Management of Healthy Behaviors in Diabetes, Kidney Disease, and Hypertension
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Pennsylvania |
| Enrollment | 73 |
| Study Type | INTERVENTIONAL |
| Conditions | Renal Insufficiency, Chronic; Hypertension; Diabetes |
| Interventions | ; |
The planned intervention, entitled, Supporting Self-Management of Health Behaviors to Optimize Health (SMART-HABITS for Health), aims to provide support for patients with chronic kidney disease (CKD), hypertension and diabetes by providing text messages delivered as motivational reminders and support to encourage blood pressure self-monitoring through goal setting, customized task prompts via t…
NCT05636826 — Olive Leaf Extracts in the Control of Hypertension
| Status | Completed |
| Phase | Phase 2 / Phase 3 |
| Sponsor | University of Monastir |
| Enrollment | 500 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension |
| Interventions | ; |
This study will be carried out in 2 emergency departments (at the exit of the emergency room) and 2 external consultations (endocrinology of the CHU FB Monastir and diabetology consultation, Jemmal hospital).
Patients over 18 years of age with:
Arterial hypertension (hypertension).
NCT06174766 — A Study to Evaluate Efficacy and Safety of HGP2102 in Essential Hypertension Patients
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Hanmi Pharmaceutical Company Limited |
| Enrollment | 356 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension |
| Interventions | ; ; |
A Multicenter, Randomized, Double-blind, Phase 3 Study to Evaluate the Efficacy and Safety of HGP2102 in patients with Essential Hypertension
NCT06960629 — The Effect of ROCK Inhibitors on Corneas of Patients With Glaucoma and Pseudophakic Bullous Keratopathy (PBK)
| Status | Completed |
| Phase | Phase 2 / Phase 3 |
| Sponsor | University Hospital Dubrava |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Pseudophakic Bullous Keratopathy; Glaucoma |
| Interventions | ; |
The goal of this clinical trial is to learn if topical netarsudil/latanoprost works to treat pseudophakic bullous keratopathy in patients with glaucoma. The main questions it aims to answer are:
Does topical netarsudil/latanoprost improves visual function in patients with glaucoma and pseudophakic bullous keratopathy? Does topical netarsudil/latanoprost affects the central corneal thickness (C…
NCT07688824 — The Effect of SPU on Hormonal and Cardiometabolic Factors
| Status | Completed |
| Phase | N/A |
| Sponsor | King Abdullah University Hospital |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypothyroidism; Hypertension; Healthy Adult; Diabete Mellitus; Hyperthyroidism |
| Interventions |
The study examines the immediate effect of soleus pushup exercise on cardiometabolic and hormonal functions among hypothyroid patients.
NCT06961981 — Remote Vinyasa Yoga Program for Heart Health
| Status | Completed |
| Phase | N/A |
| Sponsor | West Virginia University |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension; Cardiovascular Diseases |
| Interventions |
The purpose of this study is to test a 12-week vinyasa yoga (flow yoga) intervention via Zoom. This program will be for 30 individuals with high blood pressure. 15 will receive the intervention and 15 will follow their usual routine. The investigators will determine if this vinyasa yoga program is feasible and acceptable in this population. Investigators will measure and compare blood pressure …