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Stroke clinical trials

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NCT ID: NCT01275495 Completed - Stroke Clinical Trials

Telephone Assessment and Skill-Building Intervention for Stroke Caregivers

TASKII
Start date: May 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the efficacy of the revised Telephone Assessment and Skill-Building Kit (TASK II) compared with an Information, Support, and Referral (ISR) intervention in family caregivers of stroke survivors. We will also test if TASK II intervention effects on primary outcomes (depressive symptoms, caregiving-related negative life changes, unhealthy days) are mediated through effects on secondary outcomes (task difficulty, optimism, threat appraisal). Comparative costs and outcomes for the TASK II and ISR interventions will also be explored.

NCT ID: NCT01275261 Terminated - Stroke Clinical Trials

Pilot Study of Avoidance of Bladder Catheters in Stroke Patients to Avoid Urinary Tract Infections

Start date: January 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether bladder catheterization can be safely avoided in patients admitted to the hospital with stroke using a nursing protocol, and whether this decreases the incidence of urinary tract infections. The investigators hypothesize that the protocol will be tolerated by nurses and patients, and that patients without bladder catheters will have fewer urinary tract infections and better outcomes.

NCT ID: NCT01273935 Completed - Clinical trials for Test the Efficacy of Antiplatelet Regimes in Acute Stroke

Dose-Dependent Effect of Early Antiplatelet Therapy in Acute Ischemic Stroke

Start date: January 2010
Phase: N/A
Study type: Observational

The aim of this study is to evaluate the low-response prevalence of early antiplatelet therapy and to test the influence of different aspirin dosages in patients with acute ischemic strokes (AIS).

NCT ID: NCT01273467 Completed - Stroke Clinical Trials

A Safety and Tolerability Study of 42037788 (Referred to as CNTO 0007) Compared With Placebo in Patients Who Have Experienced Ischemic Cerebral Infarction (Also Known as Stroke)

Start date: December 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety and tolerability of 42037788 (CNTO 0007) in patients who have suffered a stroke. The study is not designed to establish efficacy, although preliminary explorations will be conducted.

NCT ID: NCT01273337 Unknown status - Stroke Clinical Trials

Study of ALD-401 Via Intracarotid Infusion in Ischemic Stroke Subjects

Start date: March 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to demonstrate the safety of the delivery of ALD-401 by intracarotid infusion and to assess efficacy of treatment in subjects who have had unilateral, predominately cortical, ischemic strokes in the middle cerebral artery (MCA). ALD-401 is made from the stroke patient's bone marrow and infused 13-19 days after the stroke.

NCT ID: NCT01270867 Completed - Ischemic Stroke Clinical Trials

Randomized Trial Evaluating Performance of the Trevo Retriever Versus the Merci Retriever in Acute Ischemic Stroke

TREVO2
Start date: February 2011
Phase: N/A
Study type: Interventional

To determine if the Trevo Retriever is as good or better than the Merci Retriever in restoring blood flow to the brain of a patient experiencing an acute ischemic stroke in a large vessel.

NCT ID: NCT01268683 Completed - Ischemic Stroke Clinical Trials

Glyburide Advantage in Malignant Edema and Stroke Pilot

GAMES-PILOT
Start date: May 26, 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The primary objective of this study is to assess the feasibility of enrolling, evaluating, and treating with glyburide for injection severe anterior circulation ischemic stroke participants, whether or not treated with standard of care intravenous (IV) recombinant tissue plasminogen activator (rtPA). Participants must be between 18-80 years of age, must have a baseline diffusion weighted image (DWI) lesion volume 82 -210 centimeters cubed (cm3), and time from symptom onset to start of study infusion must be ≤10 hour(hr). The secondary objectives are to assess the initial safety and tolerability, and pharmacokinetics (PK) /pharmacodynamics (PD) of glyburide in severe stroke participants, as well as to compare the clinical and magnetic resonance imaging (MRI) outcome data to benchmark data derived from published literature.

NCT ID: NCT01265238 Completed - Stroke Clinical Trials

Neuro-orthopaedic Surgery in the Treatment of the Spastic Equinovarus Foot

Start date: December 2009
Phase: N/A
Study type: Observational

Spastic equinovarus foot (SEF) is a major cause of disability in stroke patients. Treatments may include physical therapy, orthosis, botulinum toxin (BTX) injections, selective tibial neurotomy and tendon lengthening and/or transfer. Until now, no study has been conducted to assess the result of neuro-orthopaedic surgery in the treatment of SEF. The aim of this study is to evaluate the benefit of neuro-orthopaedic surgery (selective neurotomy and/or Achilles tendon lengthening and/or tibialis anterior transfer) in case of SEF according to the 3 domains of the International Classification of Functioning, Disability and Health (ICF)of the World Health organisation (WHO)

NCT ID: NCT01265043 Completed - Acute Stroke Clinical Trials

A Randomized Clinical Trial of Oral Health Promotion Interventions Among Patients After Stroke

Start date: July 2008
Phase: Phase 4
Study type: Interventional

The main aim of this oral health intervention project is to compare the effect of providing 1) professional oral hygiene instruction alone versus 2) professional oral hygiene instruction plus adjunctive Chlorhexidine mouth rinse versus 3) professional oral hygiene instruction plus adjunctive assisted tooth brushing and Chlorhexidine mouth rinse, on the oral health condition, the general health condition and health-related quality of life (HRQoL) of patients with stroke who are receiving hospital-based rehabilitation. An additional aim is to assess potential longer term oral intervention-related health and HRQoL outcomes.

NCT ID: NCT01264549 Completed - Ischemic Stroke Clinical Trials

Stroke Adverse Outcome is Associated With Nosocomial Infections: PCTus- Guided Antibacterial Therapy in Severe Ischemic Stroke Patients (STRAWINSKI)

STRAWINSKI
Start date: December 2010
Phase: N/A
Study type: Interventional

Development of stroke associated pneumonia (SAP) has a detrimental effect on stroke outcome. Biomarker-guided antibiotic treatment of patients at high risk for pneumonia may help to improve stroke outcome. Therefore, the investigators will evaluate whether intensified infection monitoring via Procalcitonin guiding an early standardized antibiotic treatment improves functional outcome after stroke compared with standard therapy based on current guidelines.