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Subarachnoid Hemorrhage clinical trials

View clinical trials related to Subarachnoid Hemorrhage.

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NCT ID: NCT03980613 Completed - Clinical trials for Subarachnoid Hemorrhage

Presentation of Subarachnoid Haemorrhage

Start date: August 26, 2019
Phase:
Study type: Observational

It is the primary aim of this study to identify symptoms and/or specific words (trigger words) indicative of spontaneous subarachnoid haemorrhage (sSAH) during emergency telephone calls to the Emergency Medical Service Copenhagen (EMS). Further, it is the aim to determine the association between the symptoms/trigger words and sSAH, the sensitivity of the symptoms/trigger words and finally, to identify factors in the telephone visitation that may influence the level of activated prehospital response

NCT ID: NCT03894202 Completed - Clinical trials for Subarachnoid Hemorrhage

Impact of Ultra-Early Intracranial Aneurysm Treatment in SAH

UEAT
Start date: November 1, 2019
Phase:
Study type: Observational

This is the first prospective study in Hong Kong that recruit patients with poor neurological status after intracranial aneurysm rupture in all seven public neurosurgical services in Hong Kong. This study assesses whether ultra-early aneurysm treatment improves outcomes in patients with poor neurological status after intracranial aneurysm rupture in Hong Kong. These data are essential to understand the impact of the disease and for future service development in Hong Kong.

NCT ID: NCT03801694 Completed - Clinical trials for Acute Ischemic Stroke

Predicting the Development of Myocardial Depression in Acute Neurological Patients

Start date: December 3, 2018
Phase:
Study type: Observational

The purpose of this study is to assess the levels of serum catecholamines associated with myocardial depression (MD) in patients with acute neurological injury.

NCT ID: NCT03786068 Completed - Clinical trials for Spontaneous Subarachnoid Hemorrhage

Time to Specialized Admission in Case of Severe Brain Haemorrhage.

Start date: January 21, 2019
Phase:
Study type: Observational [Patient Registry]

Spontaneous subarachnoid haemorrhages (SAH) are a particularly severe type of stroke with a tendency to affect younger individuals than other types of stroke. The condition is time critical as early neurosurgical treatment is needed. The aim of this study is to determine the delay from when a patient with SAH calls the Emergency Medical Services (EMS) to they are admitted to a neurosurgical department. Further, it is the aim to determine predictors for increased delay and to examine the accuracy of the triage tool used by the EMS.

NCT ID: NCT03761654 Completed - Clinical trials for Left Ventricular Dysfunction

Detection of Myocardial Dysfunction in Non-severe Subarachnoid Hemorrhage (WFNS 1-2) Using Speckle-tracking Echocardiography (STRAIN)

SAH-STRAIN
Start date: January 2, 2019
Phase:
Study type: Observational

Subarachnoid hemorrhage (SAH) can cause transient myocardial dysfunction. Recently, it have been reported that myocardial dysfunctions that occur in SAH are associated with poor outcomes. It therefore appears essential to detect theses dysfunctions with the higher sensitivity as possible. Strain measurement using speckle-tracking echocardiography may detect myocardial dysfunction with great sensitivity. The main objective of this study is to assess the prevalence of myocardial dysfunction in "non-severe" SAH (defined by a WFNS grade 1 or 2), using speckle-tracking echocardiography. This study also aims to analyse Strain measurement with classical echocardiography and serum markers (troponin, BNP) of cardiac dysfunction.

NCT ID: NCT03754335 Completed - Headache Clinical Trials

SubArachnoid Hemorrhage HEadache Treated by Lumbar Puncture

SAH-HELP
Start date: November 28, 2018
Phase: N/A
Study type: Interventional

Headache control is one of the major challenges in patients who suffered an acute aneurysmal subarachnoid hemorrhage (aSAH). Headache affects 90% of the patient and is resistant to the major pain medication. It results from the increased intracranial pressure and the inflammation caused by the accumulation of arterial blood in the subarachnoid space. Hemorrhagic cerebrospinal fluid (CSF) removal by a lumbar puncture (LP), is well tolerated, reduces intracranial pressure and accelerates the clearance of the blood products from CSF. Nonetheless it has never been tested in a randomized trial. The investigators aim to compare in patients who experienced a low grade aSAH, the variation of headache intensity after CSF removal by LP vs. Sham LP in addition to predefined analgesic protocol management.

NCT ID: NCT03710278 Completed - Clinical trials for Subarachnoid Hemorrhage

The Effectiveness and Safety of Human Lumbar Puncture Assist Device (LPat)

LPat
Start date: December 21, 2017
Phase:
Study type: Observational

The purpose of this study is to proof and investigate the effectiveness and safety of the invented device named "Human Lumbar Puncture Assist Device (LPat)" as an assist tool to be utilized to improve the success rate of performing lumbar puncture (LP), avoid side effects from multiple punctures, avoid excess radiation if the LP need to be done under fluoroscopy, and need to obtain none traumatic tap for better CSF analysis.

NCT ID: NCT03691727 Completed - Clinical trials for Subarachnoid Hemorrhage, Aneurysmal

Induced Suppression of Platelets Activity in Aneurysmal SAH Management (iSPASM)

Start date: January 24, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

This is a phase 1/2a, randomized, double blind, single-center study comparing standard care alone to standard care with Aggrastat in patients diagnosed with aneurysmal subarachnoid hemorrhage.

NCT ID: NCT03607825 Completed - Clinical trials for Subarachnoid Hemorrhage

FILtration of Subarachnoid Hemorrhage Via SpinaL CAtheteR Extension

PILLAR-XT
Start date: December 25, 2018
Phase: N/A
Study type: Interventional

The objective of this study is to further demonstrate safety and characterize effectiveness of the Neurapheresis™ System (extracorporeal system and catheter) to remove red blood cells (RBCs) and lysed blood by-products from hemorrhagic cerebrospinal fluid (CSF) following aneurysmal subarachnoid hemorrhage (aSAH).

NCT ID: NCT03585270 Completed - Clinical trials for Aneurysmal Subarachnoid Hemorrhage

Clinical Research Study With Clazosentan to Evaluate Its Effects on Preventing Complications Due to the Narrowing of the Blood Vessels (Vasospasm) in the Brain, Caused by Bleeding Onto the Surface of the Brain

REACT
Start date: February 3, 2019
Phase: Phase 3
Study type: Interventional

This study will evaluate if clazosentan (on top of normal routine medical care) can reduce the risk of developing complications related to cerebral vasospasm and permanent brain damage as compared to normal routine medical care alone.