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Endovascular Procedures clinical trials

View clinical trials related to Endovascular Procedures.

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NCT ID: NCT05049564 Completed - Clinical trials for Intracranial Aneurysm

Comparison of Clipping Via Keyhole Versus Traditional Approaches and Coiling for Ruptured Aneurysms

Start date: January 1, 2013
Phase: N/A
Study type: Interventional

Endovascular coiling has become a strategy of choice of intracranial aneurysms due to its minimally invasiveness. However, there has few prospective randomized controlled studies on the comparison of therapeutic effect between endovascular coiling and microsurgical clipping, especially the latter via keyhole approaches, which has been widely used in recent years. Based on the data of a single center, a randomized controlled study was conducted on patients with ruptured anterior circulation aneurysms suitable for both endovascular and extravascular treatment, including endovascular coiling, microsurgical clipping via conventional craniotomy and keyhole approaches, in order to compare the efficacy of the above strategies and provide more objective basis for treatment selection for operators.

NCT ID: NCT04099615 Completed - Clinical trials for Endovascular Procedures

PROMISE (Somatosensory Evoked POtEntials MonItoring During Acute Ischemic StrokE) Study

PROMISE
Start date: January 1, 2018
Phase:
Study type: Observational [Patient Registry]

Endovascular treatment in patients with acute ischemic stroke due to large vessel occlusion does not always lead to good clinical and functional outcome, despite achieving complete arterial recanalization. The rate of significant functional disability or death after three months of an acute ischemic stroke still ranges from 40% to 67%. There is experimental and clinical evidence that somatosensory evoked potentials (SEPs) are good indicators of cerebral blood flow. The primary objective of this study is to determine the sensitivity and specificity of N20 response of SEPs prior to mechanical thrombectomy (MT) as a predictor of functional independence at 90 days after endovascular treatment. Secondly, the investigators will study whether SEPs may be neurophysiological markers of brain tissue in ischemic penumbra and optimal collateral circulation. Bilateral median nerve SEPs will be recorded before and continuously during MT in patients with acute ischemic stroke and anterior large vessel occlusion. N20 response ipsilateral to the cerebral hemisphere affected will be measured (qualitatively and quantitatively). The adjusted predictive value of the N20 biomarker on functional independence after MT will be analyzed by binary logistic regression and its predictive value on the full range of disability by ordinal logistic regression. The investigators will construct different regression models with other clinical predictors available at the prehospital setting and with those determined after hospital admission to determine the independent predictive power of the N20 response for a potential treatment decision-making. Finally, the investigators will study whether SEP can be neurophysiological markers ischemic penumbra tissue and optimal collateral circulation through its correlation with multimodal neuroimaging techniques. SEPs recording is non-invasive technique that can be performed at the bedside of the patient. The development of a portable device which could allow SEPs recording by sanitary staff (pre- and intrahospitally) would provide early data about N20 value, speeding up streamline decision making.

NCT ID: NCT03875846 Completed - Blood Pressure Clinical Trials

Intraoperative Simultaneous Pressure Guided Revascularization Study

INSTANT
Start date: October 1, 2018
Phase:
Study type: Observational

This study aims to determine whether intraoperative physiologic measurements of blood flow to the leg during endovascular treatment of Peripheral Arterial Disease (PAD) can predict future clinical outcomes.

NCT ID: NCT03621202 Completed - Clinical trials for Endovascular Procedures

Safety and Accuracy of the Saranas EBBMS for the Detection of Endovascular Procedure Related Bleeding Events

Start date: August 13, 2018
Phase: N/A
Study type: Interventional

To evaluate the safety and accuracy of the Saranas EBBMS for the detection of access site related internal bleeding events during large-bore endovascular procedures.

NCT ID: NCT03581409 Completed - Clinical trials for Endovascular Procedures

Comparison of Two Different Antiplatelet Preparations for an Unruptured Intracranial Aneurysm

Start date: October 24, 2018
Phase: Phase 4
Study type: Interventional

Perform a randomized comparison study of dual-antiplatelet (aspirin, prasugrel) and triple-antiplatelet (aspirin, clopidogrel, and cilostazol) preparation using P2Y12 assay in patients with high on-treatment platelet reactivity undergoing stent-assisted coil embolization for an unruptured intracranial aneurysm

NCT ID: NCT03359252 Completed - Headache Clinical Trials

Headache After Coil Embolization for Unruptured Intracranial Aneurysms

Start date: June 5, 2018
Phase: N/A
Study type: Interventional

Perform a prospective cohort study to compare the incidence and severity of headache between non-stent assisted coiling and stent assisted coiling of unruptured intracranial aneurysms.

NCT ID: NCT03105154 Completed - Clinical trials for Endovascular Procedures

Groin Wound Infection Rate Using Prevena Compared to Standard Dressing in Vascular Surgery Patients With High Risk

PREVENA
Start date: February 2016
Phase: N/A
Study type: Interventional

Evaluate wound healing using Prevena compared to standard dressings in high risk patients after vascular surgery.