Clinical Trials Logo

Hemorrhage clinical trials

View clinical trials related to Hemorrhage.

Filter by:

NCT ID: NCT02155725 Completed - Clinical trials for Post-Partum Hemorrhage

Fibrinogen in Haemorrhage of Delivery

FIDEL
Start date: April 10, 2014
Phase: Phase 4
Study type: Interventional

The purpose of the study is to assess the benefits of a therapeutic strategy that associates an early administration of human fibrinogen concentrate in the management of PPH on the reduction of bleeding after the initiation of prostaglandins intravenous infusion, following vaginal delivery.

NCT ID: NCT02153593 Terminated - Blood Loss Clinical Trials

Postoperative Bleeding Prevention in Massive Bone Tumour Resection

TRANEXTUM
Start date: March 2013
Phase: Phase 3
Study type: Interventional

Massive bone tumour resection is often associated with important postoperative bleeding. This may determine systemic (anaemia), as well as local complications (wound healing, seroma, haematoma). The objective of this study is to determine whether the use of topical tranexamic acid or topical Evicel® will reduce the perioperative bleeding comparing it with usual haemostasis.

NCT ID: NCT02152904 Completed - Clinical trials for Peptic Ulcer Bleeding

Risk Factors of Rebleeding After Peptic Ulcer Bleeding: a Nationwide Cohort Study

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

The purpose of the investigators study is to investigate the factors associated with rebleeding in patients with peptic ulcer bleeding.

NCT ID: NCT02150941 Terminated - Clinical trials for Gastrointestinal Hemorrhage

Effectiveness Study of the BioVac Direct Suction Device in Upper Gastrointestinal Bleeding

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

Upper endoscopy is performed for upper gastrointestinal bleeding (bleeding in the esophagus, stomach, or part of the duodenum) to identify and potentially treat the cause of bleeding. However, blood clots often make visualization difficult during endoscopy. The current practice is to try to wash off and suction up these blood clots with the endoscope. However, this is often not successful due to blood clots blocking the suction channel. A new device has been approved by Health Canada that attaches to the endoscope and helps prevent blockage. It is believed that this device will help doctors suck out blood clots and potentially improve visualization, identification of the cause of bleeding, and possibly health outcomes, although this has never been proven. The purpose of the this clinical trial is to test whether the device works and whether it can help patients with this type of bleeding.

NCT ID: NCT02150720 Completed - Hip Fracture Clinical Trials

Prevention of Postoperative Bleeding in Subcapital Femoral Fractures

TRANEXFER
Start date: February 2013
Phase: Phase 3
Study type: Interventional

The main hypothesis of this clinical trial is that the use of intra-articular tranexamic acid and the fibrin glue plus usual hemostasis will reduce at least a 25% the postoperative blood loss with respect to usual hemostasis in patients undergoing subcapital femoral fractures.

NCT ID: NCT02150447 Terminated - Gastric Cancer Clinical Trials

The Use of Proton Pump Inhibitor on the Prevention of Gastric Cancer Bleeding

Start date: June 2009
Phase: Phase 3
Study type: Interventional

The aim of this study is the effect of proton pump inhibitor (PPI) with respect to gastric cancer bleeding in inoperable patients.

NCT ID: NCT02149472 Completed - Clinical trials for Postpartum Haemorrhage

Towards Better Prognostic and Diagnostic Strategies for Haemostatic Changes During Major Obstetric Haemorrhage

TeMpOH-2
Start date: February 4, 2015
Phase:
Study type: Observational

Major obstetric haemorrhage (MOH) remains a cause of significant maternal morbidity and mortality worldwide. By identifying women with a higher a priori risk of major haemorrhage during their pregnancy or early during postpartum haemorrhage extra measures to prevent MOH can be taken. In this study the investigators aim to identify haemostatic parameters that during the course of haemorrhage are responsible for the on-going towards major bleeding. By doing this, cut-off points can be defined for future interventions aiming to stop this bleeding process in an early stage. Traditional coagulation parameters are currently not useful for clinical decision making, because of long turn around times. Therefore the added value of available coagulation 'point of care' tests will be evaluated during obstetric haemorrhage.These Point-of-Care (POC) tests could lead to a goal-directed haemostatic therapy for obstetric haemorrhage. A cohort of 9.500 pregnant women will be followed during their pregnancy and delivery. From all women a bleeding score will be obtained during their pregnancy by means of a validated questionnaire. The predictive value of this bleeding score for the occurrence of major obstetric haemorrhage will be evaluated. If postpartum haemorrhage develops (blood loss) > 1000 cc, blood samples will be drawn for conventional haemostatic parameters and ROTEM profiles. The pathway between minor bleeding and major bleeding will be elucidated. Interchangeability and comparability of conventional haemostatic parameters and ROTEM profiles will also be evaluated. The overall goal of the investigators is becoming more able to predict major obstetric haemorrhage in an early stage of postpartum haemorrhage and define thresholds for goal-directed hemostatic therapies.

NCT ID: NCT02149303 Completed - Atrial Fibrillation Clinical Trials

Management of Major Bleeding Events in Atrial Fibrillation Patients Using Pradaxa

Start date: June 2014
Phase: N/A
Study type: Observational

This study is being conducted to collect data on the management of major bleeding events occurring in patients with atrial fibrillation taking dabigatran etexilate.

NCT ID: NCT02147769 Completed - Clinical trials for Intraventricular Hemorrhage of Prematurity

Cerebral Oxygenation and Autoregulation in Preterm Infants

Early NIRS
Start date: May 2014
Phase:
Study type: Observational

Premature infants are at high risk for variations in blood pressure and oxygenation during the first few days of life. The immaturity of the premature brain may further predispose these infants to death or the development of neurologic problems. The relationship between unstable blood pressure and oxygen levels and brain injury has not been well elucidated. This study investigates the utility of near-infrared spectroscopy (NIRS), a non-invasive oxygen-measuring device, to identify preterm infants at highest risk for brain injury or death.

NCT ID: NCT02147197 Completed - Leiomyoma Clinical Trials

A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal Acetate for the Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas

Start date: March 31, 2014
Phase: Phase 3
Study type: Interventional

This study will evaluate the superiority of ulipristal acetate versus placebo for the treatment of abnormal uterine bleeding associated with uterine fibroids