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Subarachnoid Hemorrhage clinical trials

View clinical trials related to Subarachnoid Hemorrhage.

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NCT ID: NCT02557607 Recruiting - Clinical trials for Subarachnoid Hemorrhage

Quantification of Cerebral Blood Flow by Arterial Spin Labeling in Vasospasm in Subarachnoid Haemorrhage

ASL-HSA
Start date: December 2014
Phase: N/A
Study type: Interventional

A technique of MRI infusion -l'Arterial Spin Labeling-, non-invasive and non-irradiating, repeatable over time, appears promising in the field. This sequence allows for routine, generate perfusion maps relating to the entire brain volume

NCT ID: NCT02549716 Terminated - Stroke Clinical Trials

Clinical, Pharmacological and Molecular Effects of IV and Oral Acetaminophen in Adults With aSAH

aSAH
Start date: January 5, 2017
Phase: Phase 4
Study type: Interventional

This study compares the bioavailability of IV and PO acetaminophen in both blood and the cerebrospinal fluid (CSF) of patients following subarachnoid hemorrhage. The study will also compare the temperature and levels of inflammatory cytokines in both blood and CSF of patients treated with IV and PO acetaminophen.

NCT ID: NCT02544256 Withdrawn - Clinical trials for Subarachnoid Hemorrhage, Aneurysmal

Mild Hypothermia During Intracranial Aneurysm Clipping

Start date: December 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether mild hypothermia causes reduction of vasoconstriction in microcirculation after clipping of aneurysms, and affects the blood flow in small diameter arteries at operating site (ischemia-hyperemia) and occurrence of vasospasms during the period of 14 postoperative days measured by transcranial Doppler.

NCT ID: NCT02540005 Completed - Clinical trials for Aneurysmatic Subarachnoid Haemorrhage

Coagulation Disorders After Aneurysmatic Subarachnoid Haemorrhage

Start date: September 2015
Phase: N/A
Study type: Observational

The main purpose of this study is to analyse the on-going coagulation process after aSAH. For investigation the investigators use the rotational thromboelastometry (ROTEM) which is a point-of-care test using a variety of activators to provide a targeted and a dynamic analysis of coagulation cascade. This is a prospective, observational clinical study done in 16 aSAH patients treated in Tampere University Hospital intensive care unit and 16 control patients (elective craniotomy due to non-ruptured intracranial aneurysm.

NCT ID: NCT02503527 Terminated - Clinical trials for Aneurysmal Subarachnoid Hemorrhage

Efficacy and Safety Study of a Low-carbohydrate Tube Feed in Critically Ill Patients Under Insulin Therapy

Start date: August 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the efficacy and safety of a diabetes-specific tube feed in comparison to an isocaloric, isonitrogenous standard enteral formula in critically ill patients receiving insulin treatment for blood glucose management.

NCT ID: NCT02501434 Suspended - Clinical trials for Intracranial Aneurysm

Aneurysmal Subarachnoid Hemorrhage Trial RandOmizing Heparin

ASTROH
Start date: April 2016
Phase: Phase 2
Study type: Interventional

A Blind-adjudication Multi-center Phase II Randomized Clinical Trial of Continuous Low-dose Intravenous Heparin Therapy in Coiled Low-grade Aneurysmal Subarachnoid Hemorrhage Patients with Significant Hemorrhage Burden. - STUDY IS TEMPORARILY SUSPENDED WITH PLAN TO RESUME SOON. NO SAFETY CONCERNS

NCT ID: NCT02483351 Completed - Clinical trials for Subarachnoid Hemorrhage

Aneurysmal Subarachnoid Hemorrhage: Red Blood Cell Transfusion and Outcome

SAHaRA Pilot
Start date: October 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine the feasibility of conducting a large trial examining the effect on clinical outcome of a liberal red blood cell (RBC) transfusion strategy compared to a restrictive strategy (usual care) in patients with aneurysmal subarachnoid hemorrhage (SAH).

NCT ID: NCT02482883 Completed - Clinical trials for Subarachnoid Haemorrhage (SAH)

Evaluation of Transcutaneous Trigeminal Nerve Stimulation for Prevention of Cerebral Vasospasm After Subarachnoid Haemorrhage

TRIVASOSTIM
Start date: September 2015
Phase: N/A
Study type: Interventional

Subarachnoid haemorrhage (SAH) secondary to ruptured aneurysm represents 5 to 15% of all cases of stroke. The mortality rate of SAH is 40% and the risk of serious neurological sequelae among survivors is 10 to 20%.The causes of morbidity and mortality are mainly related to the initial damage induced by SAH and delayed cerebral ischaemia (DCI), which is generally secondary to cerebral vasospasm. Cerebral vasospasm is one of the main factors of poor prognosis after SAH, as it is associated with a 1.5- to 3-fold increase in the mortality rate during the 2 weeks following SAH in these patients. Despite a significant improvement in the time to management of this disease and the fact that the ruptured aneurysm is very often rapidly excluded by surgical or endovascular intervention, patients who survive the initial SAH remain at risk of severe complications over the following 2 weeks. Vascular stenosis of an arterial segment, called cerebral vasospasm, is observed in more than 70 to 95% of cases on digital subtraction angiography between the 7th and 14th days after ruptured aneurysm. This angiographic vasospasm can be responsible for cerebral infarction in 52 to 81% of cases. Despite 50 years of research, no clearly demonstrated effective treatment for vasospasm is currently available. This is a multicentre, randomized, comparative study, including 364 patients during the acute phase following ruptured aneurysm, in whom management is very often limited to control of complications, after exclusion of the aneurysm. The objective of this study is to validate the efficacy of transcutaneous trigeminal nerve stimulation for the prevention of vasospasm and limitation of the consequences of delayed cerebral ischaemia after SAH. This is an innovative project, as it comprises intervention in these patients prior to the development of complications and could limit the development of these complications. The prevention tool, based on external facial nerve stimulation, is a totally innovative, reversible and noninvasive technique. Use of nerve stimulation in this indication has never been previously reported and could radically modify the intensive care management of this disease over the years to come.

NCT ID: NCT02432157 Recruiting - Clinical trials for Subarachnoid Hemorrhage

Safety and Feasibility of Hypertonic Saline Solution After Aneurysmal Subarachnoid Hemorrhage:

HS3
Start date: January 2015
Phase: Phase 1/Phase 2
Study type: Interventional

Subarachnoid hemorrhage (SAH) occurs after rupture of cerebral aneurysms. Treatment of SAH focuses on avoiding medical complications including cerebral vasospasm, which may result in limited circulation to the brain. Cerebral vasospasm, or thinning of the arteries of the brain, is a feared complication that could potentially cause stroke and worst outcomes after SAH. Hypertonic saline (HTS) is a compound that may be used to prevent vasospasm following SAH by enhancing the circulation in the brain. This study will evaluate if a protocol of volume expansion with HTS is safe and effective in patients with subarachnoid hemorrhage for the prevention of cerebral vasospasm.

NCT ID: NCT02426827 Withdrawn - Cerebral Vasospasm Clinical Trials

Cervical Spinal Cord Stimulation in Cerebral Vasospasm

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

The study is a non-blinded evaluation of the use of cervical spinal cord stimulation (SCS) for treatment of patients with Hunt and Hess grade 1-2 subarachnoid hemorrhage and evidence of cerebral vasospasm.