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Subarachnoid Hemorrhage clinical trials

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NCT ID: NCT02411266 Completed - Clinical trials for Ischemic Preconditioning

Preconditioning With Limb Ischemia for Subarachnoid Hemorrhage

PreLIMBS
Start date: July 30, 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to learn about protecting the brain from dangerous low blood flow.

NCT ID: NCT02397759 Recruiting - Clinical trials for Subarachnoid Hemorrhage (SAH) From Ruptured Aneurysm

Metabolomic Profile and Proteasic Activity as Biomarkers for Early Detection of Arterial Vasospas in Arterial Vasospasm After Aneurysmal Subarachnoid Hemorrhage

Start date: November 2013
Phase: N/A
Study type: Interventional

The subarachnoid hemorrhage (SAH) from ruptured aneurysm is a situation that is life-threatening, which is largely dependent on the occurrence of vasospasm from the 4th day after the bleeding. This vasopasm is responsible of clinical morbidity in 30 to 50% of patients. It occurs in 40% of patients with severe SAH. Despite knowing this, the clinician has no biomarker for identifying patients at risk. The project presented is original and includes a screening method without a priori to identify predictive biomarkers of vasospasm, likely to become therapeutic targets. In secondary objective we will focus on the protease activity of cerebrospinal fluid (CSF) and blood as a biomarker potential of vasoconstriction at the waning of subarachnoid hemorrhage. This study will take place over a year prospectively. The inclusion of patients will be in the SAR 1 Hospital of Timone. Patients with severe severe SAH by rupture requiring the establishment of an external ventricular derivation (EVD) will be divided into two groups and compared to one group of patients without necessitating a EVD subarachnoid hemorrhage. - Group 1: Patients with vasopasm - Group 2: Patient presenting no vasopasm Detection of vasopasm was defined using a consensual definition. CSF samples (through EVD) and blood will be made upon arrival of the patient in intensive care and then between the 3rd and 4th day. As the main criterion, we will identify biomarkers of vasospasm in blood and CSF without a priori assumption by metabolomics. Analysis will be by chromatography system coupled to a high resolution mass spectrometer. This method does not justify effective calculation because it is a step of generating hypotheses requiring further biological validation based on the identified targets. The secondary criteria, we will study in the blood and CSF association between matrix metalloproteinases (MMP) 2 and 9 and the occurrence of vasopasm. RESULTS: After comparative analysis of groups 1 and 2 in two phases of the study, we will define a metabolic profile that could identify predictive biomarkers vasopasm.

NCT ID: NCT02389634 Completed - Clinical trials for Subarachnoid Hemorrhage

Identification of Novel Molecular Markers for Vasospasm

Start date: September 2010
Phase:
Study type: Observational

The purpose of the study is to identify novel genetic and protein markers for the process of cerebral vasospasm following aneurysmal subarachnoid hemorrhage.

NCT ID: NCT02381522 Completed - Brain Aneurysms Clinical Trials

Remote Ischemic Pre-conditioning in Subarachnoid Hemorrhage

RIPC-SAH
Start date: March 1, 2015
Phase: N/A
Study type: Interventional

The purpose of the study is to investigate if briefly stopping blood flow to the patient's leg will lead to the patient's body being better able to tolerate possible decreased blood flow to regions of the brain which otherwise frequently happens after subarachnoid hemorrhage. Previous studies show that various organs such as the heart, brain or kidney can tolerate longer periods of decreased blood flow if prior to that insult shorter periods of decreased blood flow were experienced.

NCT ID: NCT02377167 Completed - Clinical trials for Ischemic and Hemorrhagic Stroke, Subarachnoid Hemorrhage

Early Tracheostomy in Ventilated Stroke Patients 2

SETPOINT2
Start date: May 2015
Phase: N/A
Study type: Interventional

Patients with severe ischemic and hemorrhagic strokes, who require mechanical ventilation, have a particularly bad prognosis. If they require long-term ventilation, their orotracheal tube needs to be, like in any other intensive care patient, replaced by a shorter tracheal tube below the larynx. This so called tracheostomy might be associated with advantages such as less demand of narcotics and pain killers, less lesions in mouth and larynx, better mouth hygiene, safer airway, more patient comfort and earlier mobilisation. The best timepoint for tracheostomy in stroke, however, is not known. Preliminary data from a pilot study of early tracheostomy in patients with hemorrhagic or ischemic stroke suggest that such patients may also have improved survival and long-term functional outcomes, but a large, multicenter clinical trial is needed to confirm these findings.

NCT ID: NCT02350335 Completed - Clinical trials for Aneurysmal Subarachnoid Hemorrhage

Transdermal Nicotine Replacement in Smokers With Acute Aneurysmal Subarachnoid Hemorrhage

NRT-SAH
Start date: January 2011
Phase: N/A
Study type: Interventional

All patients with acute aneurysmal hemorrhage are treated in accordance with our institutional protocol. After securing of the aneurysm, some smokers with acute aneurysmal hemorrhage are randomly assigned to transdermal nicotine replacement (NRT). The short- and long-term effect of NRT will be studied comparing non-smokers, smokers without NRT and smokers with NRT.

NCT ID: NCT02334657 Completed - Clinical trials for Subarachnoid Hemorrhage

Prospective Study of Long-term Outcome After Non-aneurysmal Subarachnoid Hemorrhage

Start date: November 2013
Phase: N/A
Study type: Observational [Patient Registry]

Spontaneous subarachnoid hemorrhage (SAH) is usually caused by rupture of an intracranial aneurysm, but in up to 15% of patients with spontaneous SAH, no discernible bleeding source can be identified despite of repetitive radiological imaging. Patients, at least 18 months after ictus of a non-aneurysmal SAH, received a regular mail including a letter explaining the study purpose and the postal questionnaire consisting a short-form health survey with 36 simple questions. If we didn't receive answers after three months we made telephone interviews with the patients' family members or their general practitioner.

NCT ID: NCT02330094 Completed - Clinical trials for Aneurysmal Subarachnoid Hemorrhage

Gabapentin for Headache in Aneurysmal Subarachnoid Hemorrhage

Start date: December 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to see how much gabapentin will reduce headaches associated with subarachnoid hemorrhage (SAH) and to reduce the amount of narcotic pain medication prescribed.

NCT ID: NCT02323685 Completed - Cerebral Ischemia Clinical Trials

Safety and Effect of SANGUINATEā„¢ Infusion in Patients at Risk of Delayed Cerebral Ischemia (DCI) Following Subarachnoid Hemorrhage (SAH)

Start date: December 2014
Phase: Phase 2
Study type: Interventional

Safety and effect of SANGUINATE on patients DCI following SAH.

NCT ID: NCT02320539 Completed - Clinical trials for Subarachnoid Hemorrhage

MicroRNA Diagnostics in Subarachnoid Hemorrhage 2

Start date: November 2014
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to validate results from a related trial (NCT01791257) and to compare the profile of microRNA in blood from patients suffering subarachnoid hemorrhage with and without systemic complications.