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Coronary Vasospasm clinical trials

View clinical trials related to Coronary Vasospasm.

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NCT ID: NCT02057783 Recruiting - Sleep Apnea Clinical Trials

Physical Activity Program for Reducing Blood Pressure in Sleep Apnea Patients With Resistant Hypertension

RAP
Start date: March 26, 2015
Phase: N/A
Study type: Interventional

Investigators hypothesize that CPAP treatment for suppressing OSAS in combination with a physical activity program will optimize 24-hour blood pressure control in patients with OSA-related resistant hypertension.

NCT ID: NCT02042066 Not yet recruiting - Clinical trials for Hypertension, Resistant to Conventional Therapy

Safety and Efficacy Study of Extracorporeal Shockwave Therapy in the Treatment of Patients With Resistant Hypertension

RHT
Start date: January 2015
Phase: Phase 1
Study type: Interventional

Low intensity shockwaves have been proven in animal and human studies to increase tissue perfusion, promote angiogenesis and tissue regeneration and improve neural function. The hypothesis of this study is that shockwave therapy could improve the symptoms of patients with resistant hypertension.

NCT ID: NCT01904695 Completed - Clinical trials for Hypertension, Resistant to Conventional Therapy

Causal Inference Research of Resistant Hypertension Treatment With Chinese Approach in a Cohort Study

Start date: August 2013
Phase: Phase 0
Study type: Interventional

The research of clinical effectiveness assessment is to explore the causal relationship between treatment and outcome.Accordingly, based on the effectiveness of tan-yu treatment, the research takes the Resistant Hypertension (RH) as example to study the causal inference methods under real world.

NCT ID: NCT01882790 Completed - Hypertension Clinical Trials

The Prevalence of Coronary Spasm in Hypertensive Patients Treated With Antihypertensive Medication

Start date: May 2013
Phase: N/A
Study type: Observational [Patient Registry]

Autonomic nerve function is involved in both blood pressure (BP) regulation and the pathogenesis of coronary artery spasm(CAS), but few studies have been published about the relationship between CAS and effect of BP lowering drugs in patients with hypertension. The purpose of this study is to investigate the incidence of CAS, atrioventricular (AV) block and effect of BP lowering drugs on CAS in hypertensive patients treated with BP lowering agents. The investigators will register consecutive patients who underwent coronary angiography with an acetylcholine (Ach)-induced provocation test. The investigators will include hypertensive patients who were taking antihypertensive drugs, and exclude patients who had a documented history of cardiovascular disease or who were not treated with antihypertensive agents. CAS is defined as >70% luminal narrowing on Ach provocation and /or concurrent chest pain. The study population will be divided into quartiles of rising systolic BP and diastolic BP. The incidence of Ach-induced CAS according to each systolic BP/diastolic BP quartile will be evaluated.

NCT ID: NCT01877993 Completed - Clinical trials for Autonomic Dysfunction

The Effect of Autonomic Function on Coronary Vasomotion

Start date: May 2013
Phase: N/A
Study type: Observational [Patient Registry]

Autonomic nerve function is involved in both blood pressure (BP) regulation and the pathogenesis of coronary artery spasm (CAS), but few studies have been published about the relationship between CAS and BP, with the exception of studies that explore hypertension as a risk factor for CAS. The purpose of this study was to investigate the incidence of CAS and atrioventricular (AV) block in association with BP level. The investigators will register consecutive patients who underwent coronary angiography with an acetylcholine (Ach)-induced provocation test from November 2004 to May 2012. The investigators exclude from the patients who were taking antihypertensive drugs or who had a documented history of cardiovascular disease in order to avoid the confounding effects of cardiovascular medications on coronary vasomotion. CAS is defined as >70% luminal narrowing on Ach provocation and /or concurrent chest pain. The study population will be divided into quartiles of rising systolic BP and diastolic BP. The incidence of Ach-induced CAS according to each systolic BP/diastolic BP quartile will be evaluated.

NCT ID: NCT01863082 Recruiting - Clinical trials for Hypertension, Resistant to Conventional Therapy

Resistant Hypertension and Physical Activity Performed in a Heated Pool

HAR
Start date: November 2011
Phase: N/A
Study type: Interventional

patients with resistant hypertension will be submitted to an exercise protocol in a heated pool for three months

NCT ID: NCT01848275 Completed - Clinical trials for Hypertension, Resistant to Conventional Therapy

Full Length Versus Proximal Renal Arteries Ablation

Start date: March 2011
Phase: N/A
Study type: Interventional

Catheter-based renal sympathetic modification has been documented to be effective option for blood pressure control in patients with resistant hypertension, but the safety is still concerned around worldwide. Based on anatomic findings, blocking renal sympathetic nerves at proximity may be enough for successful renal sympathetic modifications. This study was designed to compare the efficacy and safety of full length versus proximal ablation of bilateral renal arteries.

NCT ID: NCT01835535 Active, not recruiting - Clinical trials for Hypertension, Resistant to Conventional Therapy

Continued Safety and Performance of the TIVUS System

Start date: August 2013
Phase: Phase 2/Phase 3
Study type: Interventional

The TIVUS II is a prospective, multicenter, non-randomized, open-label clinical study of the safety and performance of the TIVUS™ System consisting of three (3) concurrent cohorts: - TIVUS™ Severe Resistant HTN Cohort - TIVUS™ Moderate Resistant HTN Cohort - TIVUS™ Failed RF Therapy Cohort

NCT ID: NCT01834118 Completed - Clinical trials for Hypertension, Resistant to Conventional Therapy

Reintervention-study After Previous Renal Denervation in Non-responding Patients With Severe Hypertension

RETREAT
Start date: June 2013
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to determine the effect of repeated renal denervation in non-responding patients with severe hypertension. Therefore ultrasound technique will be used.

NCT ID: NCT01833429 Completed - Clinical trials for Hypertension, Resistant to Conventional Therapy

Autonomic Dysfunction in Resistant Hypertension

RH
Start date: September 2011
Phase: N/A
Study type: Observational [Patient Registry]

The contribution of this study is the unedited evaluation of the circadian autonomic profiles of resistant hypertension with and without white-coat response.