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Autonomic Dysreflexia clinical trials

View clinical trials related to Autonomic Dysreflexia.

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NCT ID: NCT05380661 Recruiting - Clinical trials for Spinal Cord Injuries

Heart Rate Variability and Anxiety During Urinary Bladder Catheterization

Start date: July 15, 2022
Phase: N/A
Study type: Interventional

This is a prospective, randomised study investigating the physical and psychological experience of intermittent catheterization in adult individuals following spinal cord injury (SCI).

NCT ID: NCT05351827 Recruiting - Clinical trials for Spinal Cord Injuries

Mild Intermittent Hypoxia: A Prophylactic for Autonomic Dysfunction in Individuals With Spinal Cord Injuries

MIH and AD
Start date: October 1, 2022
Phase: N/A
Study type: Interventional

The prevalence of autonomic dysfunction and sleep disordered breathing (SDB) is increased in individuals with spinal cord injury (SCI). The loss of autonomic control results in autonomic dysreflexia (AD) and orthostatic hypotension (OH) which explains the increase in cardiovascular related mortality in these Veterans. There is no effective prophylaxis for autonomic dysfunction. The lack of prophylactic treatment for autonomic dysfunction, and no best clinical practices for SDB in SCI, are significant health concerns for Veterans with SCI. Therefore, the investigators will investigate the effectiveness of mild intermittent hypoxia (MIH) as a prophylactic for autonomic dysfunction in patients with SCI. The investigators propose that MIH targets several mechanisms associated with autonomic control and the co-morbidities associated with SDB. Specifically, exposure to MIH will promote restoration of homeostatic BP control, which would be beneficial to participation in daily activities and independence in those with SCI.

NCT ID: NCT05024487 Recruiting - Clinical trials for Spinal Cord Injuries

Prevention of Complications Due to Autonomic Dysreflexia in SCI Individuals

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

Autonomic dysreflexia (AD) is a syndrome of unbalanced response of the sympathetic system to noxious stimuli below the level of spinal cord injury (SCI), characterized by paroxysmal hypertension. Mostly, it is combined with symptoms such as pounding headache, slowed heart rate, and upper body flushing, but it can also be asymptomatic. When resulting in hypertensive crisis, it can be life-threatening and result in seizures, cardiac arrest, retinal or subarachnoid hemorrhages, stroke, and even death. The aim of this study is to determine the risk level of vascular complications in SCI people by correlating the clinical symptoms with their individual perception during AD triggered below the level of injury.

NCT ID: NCT04193709 Recruiting - Blood Pressure Clinical Trials

Recovery of Bladder and Sexual Function After Human Spinal Cord Injury

Start date: January 4, 2021
Phase: N/A
Study type: Interventional

This study will incorporate critical cross viscero-visceral intersystem interactions to 1) investigate in a controlled laboratory setting and then with mobile at-home monitoring the extent, severity, and frequency of occurrence of autonomic dysreflexia with respect to daily bladder and bowel function, in conjunction with identifying potential underlying mechanisms by examining urinary biomarkers for several specific vasoactive hormones, and 2) to regulate cardiovascular function therapeutically as part of bladder and bowel management using spinal cord epidural stimulation.

NCT ID: NCT03914677 Recruiting - Clinical trials for Spinal Cord Injuries

Mecamylamine for Autonomic Dysreflexia Prophylaxis

Start date: June 13, 2019
Phase: Phase 4
Study type: Interventional

This is a preliminary study of the antihypertensive drug mecamylamine, used in the specific circumstance of hypertension caused by autonomic dysreflexia (AD), a condition that affects people with spinal cord injury (SCI). Initially, mild sensory stimulation of subjects' legs is used to intentionally provoke AD, as reflected by blood pressure elevation during such stimulation. In subsequent testing sessions, mecamylamine is given prior to sensory stimulation, to show the effect of the drug on preventing these AD-related blood pressure elevations.