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Stroke clinical trials

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NCT ID: NCT00393926 Completed - Stroke Clinical Trials

Robot-Assisted Motivating Rehabilitation

Start date: July 2006
Phase: Phase 1
Study type: Interventional

The purpose of the study is to examine how a novel robot technology designed for eventual use as a home therapy can improve arm function after stroke.

NCT ID: NCT00391378 Completed - Stroke Clinical Trials

Cerebral Lesions and Outcome After Cardiac Surgery (CLOCS)

Start date: September 9, 2006
Phase: N/A
Study type: Observational

Between 1 and 5 percent of patients who have coronary artery bypass surgery suffer a stroke following surgery, and 30 percent have new brain lesions that do not produce symptoms and are seen only on MRI. In addition, up to 40 percent of patients develop long-term cognitive impairment. This study will identify risk factors that predict whether a person undergoing heart surgery will develop cerebral infarcts after surgery. It will also identify operative and inflammatory factors that may alter the risk, and will evaluate whether the small lesions are associated with cognitive decline at 6 months. People 18 years of age or older who will undergo coronary artery bypass surgery (CABG), heart valve replacement, or combined CABG and valve replacement procedure are eligible for this study. Candidates must have no neurological or cognitive impairment before surgery. Participants will undergo standard medical and surgical treatment as determined by their physicians. In addition, they have the following procedures: - Medical and neurological evaluation before surgery and 24 and 48 hours after surgery. - Brain MRI before surgery, and 48 hours, 30 days and 6 months after surgery. - Blood draws before surgery, immediately after surgery, and 6, 24, 48 and 72 hours after surgery to quantify the response of their inflammatory system to surgery. - Neuropsychological examinations 30 days and 6 months after surgery. - In addition, patients who agree to enroll in a substudy that will explore whether differences in the genes coding for inflammatory molecules lead to a change in the risk of iscjhemia after heart surgery, will have extra blood drawn for genetic analysis.

NCT ID: NCT00390962 Completed - Stroke Clinical Trials

The "COSMOS"-Study (Copeptin in Osmoregulation and Stress Assessment)

Start date: November 2006
Phase: N/A
Study type: Observational

Sodium imbalance is common and an adverse prognostic factor in hospitalized patients. However, identifying the causes of sodium imbalance is challenging in clinical practice. Levels of antidiuretic hormone (ADH) are elevated in patients with stroke correlating with disease severity and stress level; however, its measurement is cumbersome. ADH is derived from a larger precursor peptide along with Copeptin, which is a more stable peptide directly mirroring the production of ADH. Copeptin can be assayed readily in plasma. Early prognostic factors to predict in-hospital mortality and medium/long-term outcome in critically ill neurological patients, are helpful to guide and tailor early decisions on treatment, discharge from the intensive care unit and application of interventions to prevent deterioration of neurological functions. We hypothesize that copeptin will improve the diagnostic accuracy to diagnose sodium imbalances as compared to routinely used markers Furthermore, we hypothesize that Copeptin will be a reliable prognostic tool, dependent or independent of sodium imbalance, to predict short-term (i.e. in-hospital) and medium-term (i.e. 3 months) clinical outcome in stroke patients.

NCT ID: NCT00390286 Withdrawn - Stroke Clinical Trials

Telemedicine's Utility for Augmenting Clinical Trials and Informed Consent TACTIC

Start date: November 2016
Phase: Phase 1
Study type: Observational

This is a 6 year, Phase I, Clinical Research Protocol to study the feasibility of using a telemedicine system for performing research in a remote hospital system.

NCT ID: NCT00389467 Completed - Stroke Clinical Trials

Mechanical Retrieval and Recanalization of Stroke Clots Using Embolectomy

MR RESCUE
Start date: May 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the effectiveness of treating acute ischemic stroke with mechanical embolectomy using the Merci Retriever or the Penumbra System within 8 hours of symptom onset to standard medical treatment, and to identify people who might benefit from mechanical embolectomy by the appearance of stroke on multimodal computerized tomography (CT) or magnetic resonance (MR) imaging.

NCT ID: NCT00389012 Completed - Clinical trials for Cerebrovascular Accident

Strength Training Effectiveness Post-Stroke (STEPS)

Start date: May 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if treadmill training with body weight-support (BWST) is more effective at improving walking in individuals post-stroke than a resisted leg-cycling exercise program. In addition, we want to determine if training programs that combine leg strength training to treadmill walking provide an additional benefit to post-stroke walking outcomes.

NCT ID: NCT00387712 Completed - Stroke Clinical Trials

Inflammatory Abnormalities in Muscle After Stroke: Effects of Exercise

Start date: October 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to first define whether abnormalities of skeletal muscle are related to the presence of inflammation and to poor motor performance and whether this can be modified by exercise interventions.

NCT ID: NCT00384748 Completed - Clinical trials for Cerebrovascular Accident

Home-based Telehealth Stroke Care: A Randomized Trial for Veterans

Start date: November 2008
Phase: Phase 2
Study type: Interventional

The purpose of the proposed study is to examine a Tele-rehabilitation (TR) intervention that uses tele-health technology to improve outcomes of stroke patients after discharge to home. The primary aim is to determine the effect of TR on physical function, and secondarily to determine the effect on disability, falls-related self-efficacy, and patient satisfaction.

NCT ID: NCT00379392 Completed - Stroke Clinical Trials

Mental Imagery to Reduce Motor Deficits in Stroke

Start date: January 2003
Phase: Phase 1
Study type: Interventional

The primary aim of the proposed study is to collect data in an effort to estimate the clinical effectiveness of implementing repetitive task practice (RTP) in addition to mental imagery training (MIT) to improve upper extremity motor function and the quality of life of chronic stroke patients.

NCT ID: NCT00377689 Completed - Clinical trials for Cerebrovascular Accident

Evaluation of an Intervention Program Targeted at Improving Balance and Functional Skills After Stroke

Start date: September 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate a 5-week intervention program targeted at improving balance and functional skills for people with stroke.