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Ischemia clinical trials

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NCT ID: NCT02860260 Completed - Ischemic Stroke Clinical Trials

Kinetics of Plasma and Serum Levels of Brain-Derived Neurotrophic Factor (BDNF) in Patients With Ischemic Stroke

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

The aim of this study is to show for the first time that treatment with intravenous fibrinolysis using rt-PA in patients with recent ischemic stroke is accompanied by increases in circulating levels of BDNF, which may reflect an increase in BDNF synthesis in the brain. The analysis of the recovery of functional and cognitive abilities as well as mood at 3 months will allow us to study the impact of BDNF on these parameters. Thus, depending on the results obtained, circulating BDNF could serve as an early marker of these.

NCT ID: NCT02856074 Completed - Ischemic Stroke Clinical Trials

Functional Prognosis in Patients With Ischemic Stroke According to the Therapeutic Strategy Used

PARADISE
Start date: January 13, 2016
Phase: N/A
Study type: Interventional

The current management of ischemic stroke is based on different strategies that may be combined: intravenous thrombolysis in a stroke ICU, intravenous thrombolysis in a telemedicine procedure, endovascular thrombectomy. Given this now rich therapeutic arsenal, it seems necessary to evaluate practices in local care in the field and the impact of these on the prognosis of ischemic stroke victims. The aim of this observational study is to compare these different care practices without interfering with the choice of strategy. A blood sample will also be taken at different times to study the value of growth differentiation factors (GDF) 8, 11 and 15, and Brain-derived Neurotrophic Factor as prognostic biomarkers

NCT ID: NCT02854592 Completed - Ischemic Stroke Clinical Trials

Intravenous Thrombolysis Registry for Chinese Ischemic Stroke Within 4.5 h Onset

INTRECIS
Start date: April 1, 2017
Phase:
Study type: Observational

Stroke is one of the leading causes of death and disability in China. Intravenous thrombolysis with recombinant tissue plasminogen activator (rtPA) improves the outcome for ischemic stroke patients who can be treated within 4.5 hours of symptom onset. In China, in addition to rt-PA, intravenous urokinase within 6 h has also been recommended by the 2010 Chinese Guidelines for the Diagnosis and Treatment of Patients with Acute Ischemic Stroke, and supported by evidence from two intravenous urokinase thrombolysis trials. Urokinase is used more frequently than rt-PA, mainly because it is cheaper. To describe Chinese experience with thrombolytic therapy for Ischemic Stroke within 4.5h onset, we designed a multicenter, prospective, registry study. The aim of INtravenous Thrombolysis REgistry for Chinese Ischemic Stroke within 4.5 h onset(INTRECIS)was to assess the safety and efficacy of intravenous rtPA, urokinase as thrombolytic therapy within the first 4.5 h of onset of acute ischaemic stroke.

NCT ID: NCT02849067 Completed - Clinical trials for Ischaemic Heart Disease

Hemodynamic Responses of Stable Ischemic Heart Disease Patients to a Comedy Session

Start date: May 25, 2015
Phase: N/A
Study type: Interventional

It is known that laughter can bring benefits in terms of physiological and psychological parameters, in addition to improving the individual's quality of life. However, the literature is still scarce as to the existence of studies investigating the effects of a comedy film specifically in hemodynamics.

NCT ID: NCT02840786 Completed - Atherosclerosis Clinical Trials

Clinical Study of Stent Versus Direct Atherectomy to Treat Arteriosclerosis Occlusive Disease of Lower Extremity

Start date: January 2016
Phase: N/A
Study type: Interventional

This is a randomized study comparing stent and plaque excision systems in treatment of Arteriosclerosis occlusive disease of lower extremity (superficial femoral or popliteal artery)

NCT ID: NCT02838901 Completed - Stroke Clinical Trials

Dietary Nitrate Supplements and Ischemic Stroke Recovery

Start date: June 2012
Phase: Phase 2
Study type: Interventional

This is a double-blind, randomized, placebo-controlled, pilot study. Participants will be randomized to receive either beetroot juice or a beetroot juice placebo, as a dietary supplement, for 30 days. Beetroot juice is high in nitrates, a chemical when ingested is found to increase blood flow to the brain. The purpose of this research study is to determine the safety and feasibility of using this nutritional intervention in (ischemic)stroke survivors, and prove that plasma levels of nitrate and nitrite increase as expected. Secondary outcomes includes measuring a comprehensive set of outcomes related to functional status post-stroke, including mobility, upper extremity strength, cognition, depression, and disability. Patients will also be randomized to MRI perfusion scanning in the region of the stroke to measure cerebral blood flow.

NCT ID: NCT02835586 Completed - Critical Ischemia Clinical Trials

STREAMER : STent Restenosis And MEdicaments Release

STREAMER
Start date: May 2013
Phase: Phase 3
Study type: Interventional

It is a pilot study to evaluate the feasibility and the efficiency of local delivery of paclitaxel after stenting of long femoropopliteal arterial lesions TASC C and D before the realization of a large randomized multicentric study. Patients concerned are in critical ischemia.

NCT ID: NCT02835027 Completed - Clinical trials for Acute Ischemia of Lower Limb

Treatment of Acute Lower Limb Ischaemia in Sweden 1994-2014

Start date: January 1994
Phase: N/A
Study type: Observational [Patient Registry]

Study of acute lower ischemia therapies based on data collected from the Swedish Vascular Surgery Registry between 1994 and 2014. Primary endpoint is long term amputation-free survival and secondary end-points are 30 days and 1 year amputation-free survival as well as different revascularization techniques results and time trends.

NCT ID: NCT02834351 Completed - Clinical trials for Peripheral Artery Disease

Tissue Lesions in Exercise Related Ischemia

SARTORIUS
Start date: July 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of muscle ischemia during claudication on mitochondrial function. Comparison to patients with arterial disease but absence of lower limb claudication (Cardiac group) feasibility study.

NCT ID: NCT02834143 Completed - Stroke Clinical Trials

Evaluation of Diagnostic Criteria for Chronic Critical Limb Ischemia

CRIMI
Start date: June 13, 2014
Phase: N/A
Study type: Observational

Chronic critical limb ischemia (CCI) is the most severe clinical form of occlusive arterial disease. Its prognosis is terrible, mortality estimated at 50% in five years. However there are no recent epidemiological data on morbidity and mortality of critical ischemia. Moreover, the diagnostic criteria of the ICC associate clinical and hemodynamic criteria and are not subject to a clear consensus. Investigators propose to evaluate the validated diagnostic criteria (TASC VALMI, European working group) in a population of severe ischemia in patients in order to offer relevant simple and reproducible criteria. Secondly Investigators propose to monitor the medium and long term evolution of these patients ICC defined to clarify the prognosis. diagnostic criteria of the different societies: - TASC: Transatlantic criteria: very characteristic pain, wound optional, variable hemodynamic criteria as the presence of a wound or not - VALMI: French criteria derived vascular medical college: characteristic pain, sore, hemodynamic reproducible, reliable criteria - European working group: European definition of criteria, including a characteristic pain, requires no wound, different hemodynamic criteria of 2 others.