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Hemorrhage clinical trials

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NCT ID: NCT01098617 Recruiting - Bleeding Clinical Trials

Antihemostatic Therapy and Endoscopic Biliary Sphincterotomy Induced Bleeding

Start date: April 2010
Phase: N/A
Study type: Observational

The aim of the study is to observe the effects of antihemostatic therapy including nonsteroidal antiinflammatory, anticoagulant and antiaggregant therapy and other patient and procedure related factors on the risk of endoscopic biliary sphincterotomy induced bleeding.

NCT ID: NCT01091896 Recruiting - Clinical trials for Vitreous Hemorrhage Secondary to PDR

Adjuvant Intravitreal Bevacizumab in Pars Plana Vitrectomy for Vitreous Hemorrhage

Start date: January 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effect of pre and intra-operative bevacizumab injection on postoperative vitreous hemorrhage after diabetic vitrectomy in comparison to vitrectomy without bevacizumab injection.

NCT ID: NCT01064011 Recruiting - Clinical trials for Intraventricular Hemorrhage

Prospective Randomized, Controlled Trial for Treatment of Intraventricular Hemorrhage

IVH
Start date: January 2010
Phase: N/A
Study type: Interventional

Intraventricular hemorrhage comprises about 15% of the 500,000 strokes that occur annually in the United States. In the emergent setting, patients with obstructive hydrocephalus are routinely treated with placement of an external ventricular drain. This study will compare the effect of external ventricular drainage plus intraventricular thrombolysis versus external ventricular drainage plus endoscopic evacuation on neurologic outcomes for patients with hydrocephalus from intraventricular hemorrhage.

NCT ID: NCT00965900 Recruiting - Cirrhosis Clinical Trials

Endoscopic Band Ligation (EBL) Versus Propranolol for Primary Prophylaxis of Variceal Bleeding

Start date: September 2006
Phase: Phase 4
Study type: Interventional

This study is performed to compare the efficacy and safety of EBL, propranolol, and EBL combined with propranolol in patients with medium or large varices.

NCT ID: NCT00861640 Recruiting - Clinical trials for Nonvariceal Upper Gastrointestinal Bleeding

Comparison of Oral Rabeprazole vs. iv Omeprazole in Mild to Moderate Nonvariceal Upper Gastrointestinal Bleeding

Start date: March 2009
Phase: Phase 4
Study type: Interventional

Introduction: Proton pump inhibitor (PPI) is the drug of choice used in patients with non-variceal upper gastrointestinal tract bleeding (UGIB). Intravenous (IV) PPI is more commonly used than oral form when overt bleeding occurs. Previous study has revealed that oral rabeprazole and IV omeprazole achieved similar intragastric pH elevation. It's probable that oral form and IV PPI provide equal efficacy in treating mild to moderate UGIB patients. Aim: This study aims to compare the effect of three-day oral rabeprazole and iv omeprazole on bleeding control in patients with mild to moderate non-variceal UGIB. Patients and methods: All patients presented with black to tarry stool passage or hematemesis and visited our ER will be evaluated to recruit into this study. They will receive regular vital sign monitoring, laboratory study and nasogastric tube insertion with gastric fluid aspiration. Esophagogastroendoscopy and hemostatic procedure if need will be performed within 12 hours. Those confirmed to have non-variceal UGIB, stable vital signs and agree to participate into this study will be randomized into two groups receiving either oral rabeprazole (20mg bid) or iv omeprazole (40mg qd) for three days. The presence of recurrent bleeding within three days, in-hospital complication and duration of hospital stay will be recorded and analyzed. Expected results: At the end of this study, we will be able to determine whether patients treated with oral rabeprazole and iv omeprazole have similar re-bleeding or complication rates and hospitalization days.

NCT ID: NCT00778492 Recruiting - Bleeding Clinical Trials

Thrombelastogram in Patients Receiving Antiplatelet Medication Undergoing Cardiac Surgery

Start date: May 2008
Phase: N/A
Study type: Observational

Study Objective is to correlate the results of preoperative platelet mapping derived from modified TEG with clinically significant postoperative bleeding and consumption of blood products.

NCT ID: NCT00745758 Recruiting - Clinical trials for Subarachnoid Hemorrhage

The Factors Cause Vasospasm After Aneurysmal Subarachnoid Hemorrhage

Start date: May 2008
Phase: N/A
Study type: Observational

Extensive research has shown that the big event that leads to the initiation of vasospasm is the release of oxyhemoglobin (blood breakdown product).Depletion of NO synthase (19,20,21) was also noted after SAH.CSF is produced from choroid plexus in the ventricle. If the SAH is too dense, the blood in the subarachnoid space will not easy to be washed out.

NCT ID: NCT00713375 Recruiting - Clinical trials for Subarachnoid Hemorrhage

Time Frequency Analysis of Electrocardiogram and Blood Pressure in Intracranial Hemorrhage Patients

Start date: April 2008
Phase: N/A
Study type: Observational

Dysregulation of autonomic nervous system is evident in patients with spontaneous intracranial hemorrhage. In this study, we utilize a non-invasive method (heart rate and blood pressure variability analysis to analyze the autonomic activities in this group of neurosurgical patients. Our aim is to determine the utility of this modality in risk stratification and outcome prediction in these patients.

NCT ID: NCT00709046 Recruiting - Bleeding Clinical Trials

High Dose Versus Standard Dose Proton Pump Inhibitor (PPI) in High-risk Bleeding Peptic Ulcers After Combined Endoscopic Treatment

Start date: January 2008
Phase: N/A
Study type: Interventional

The study was designed to evaluate the efficacy an adjuvant use of standard dose or high dose of proton pump inhibitor after combined endoscopic hemostasis therapy.

NCT ID: NCT00699621 Recruiting - Clinical trials for Intracerebral Hemorrhage

Platelet Transfusion in Acute Intracerebral Hemorrhage

Start date: January 2009
Phase: N/A
Study type: Interventional

- To prove whether use of antiplatelet agents results into a rapid enlargement of hematoma after onset of acute intracerebral hemorrhage. - To prove the efficacy and safety of platelet transfusion for prevention of hematoma growth in patients who were stricken by acute intracerebral hemorrhage while being on antiplatelet medication.