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Hemorrhage clinical trials

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NCT ID: NCT01683955 Completed - Osteoarthritis, Hip Clinical Trials

Topical Tranexamic Acid and Acute Blood Loss in Total Hip Arthroplasty

Start date: January 1, 2013
Phase: Phase 1
Study type: Interventional

This study aims to assess postoperative blood loss and transfusion rates in total hip replacement after one-time administration of topical tranexamic acid.

NCT ID: NCT01678456 Completed - Atrial Fibrillation Clinical Trials

Prospective Registration and Assessment of Serious Adverse Events Within the AFNET

AFNET A7
Start date: February 2004
Phase:
Study type: Observational

Prospective registration and independent assessment of SAE associated with atrial fibrillation such as thromboembolic events, and other cardiac and noncardiac complications by a Critical Event Committee.

NCT ID: NCT01675856 Completed - Clinical trials for Gastrointestinal Bleeding

Urgent vs. Early Endoscopy in High Risk Patients With Upper Gastrointestinal Bleeding (UGIB)

Start date: July 28, 2012
Phase: N/A
Study type: Interventional

Acute upper gastrointestinal bleeding (UGIB) is one of the commonest medical emergencies. The condition accounts for 150 per 100,000 populations. A National United Kingdom reported a crude overall mortality rate of 10%. While bleeding stops spontaneously in majority of patients at their presentation, there remains a subgroup of patients who continue to bleed or develop recurrent bleeding. In these patients, the mortality increases manifolds. If these high-risk patients can be identified, early interventions may improve their outcomes. Several prognostic indices are in use for the purpose of patient stratification. They include the Rockall, Glasgow-Blatchford (GBS) and the Baylor scores. The Rockall score is a composite score which incorporates clinical parameters as well as findings during endoscopy which was derived to predict mortality. The GBS is a pre-endoscopy or a clinical score for the prediction for the need of further intervention loosely defined as the need for transfusion, endoscopy or surgery. It has been shown to be accurate in identifying low risk patients for early discharge.

NCT ID: NCT01670838 Completed - Clinical trials for Nontraumatic Subarachnoid Haemorrhage

Cardiopulmonary Complication in Aneurysmal Subarachnoid Haemorrhage Patients

SAHHEART
Start date: February 2012
Phase: N/A
Study type: Observational

This is a prospective cohort study investigating cardiac function and cardiac biomarkers in patients with acute Aneurysmal Subarachnoid Haemorrhage (aSAH). The aims of the study are to document the incidence of myocardial dysfunction,to find the predictive factors of myocardial dysfunction, describe heart rate variability and to assess the impact of all cardiac problems on morbidity and mortality.

NCT ID: NCT01668563 Recruiting - Clinical trials for Intracranial Hemorrhage Ruptured Aneurysm

International Subarachnoid Aneurysm Trial II

ISAT II
Start date: November 12, 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the clinical outcome of surgical clipping and endovascular coiling for ruptured intracranial aneurysms not included in the original ISAT Study.

NCT ID: NCT01666249 Suspended - Clinical trials for Pregnancy; Fetomaternal Hemorrhage

Clinical Efficacy of Postpartum Immunization of Rh and Coombs Negative Women With Sensitization Risk.

Start date: April 2014
Phase: Phase 3
Study type: Interventional

This a open, prospective, multicenter, single-arm, phase III study for clinical assessment of anti-Rh immunoglobulin (KamRho-D®) in Rh and Coombs negative women with risk sensitization. The anti-Rh immunoglobulin is an immunobiological containing high concentration of specific antibodies against factor D and "neutralizes" D antigen present in the Rh-positive fetal red blood cells (Rh +), which passed into the bloodstream of Rh-negative pregnant women (Rh).

NCT ID: NCT01665456 Completed - Clinical trials for Postpartum Hemorrhage

Assessing Childbirth-related Complications at the Community Level in Kenya

Start date: August 2012
Phase: N/A
Study type: Observational

Kenya is one of the countries in sub-Saharan Africa that still experience high maternal mortality. For instance, in 2008/09 maternal mortality ratio was estimated to be 488/100,000 live births. Direct obstetric complications such as puerperal sepsis, postpartum hemorrhage, pre-eclampsia and eclampsia, obstructed labor and indirect causes including HIV, malaria and anemia in pregnancy are responsible for the majority of these cases. Just under 44% of births in Kenya are delivered under the supervision of a skilled birth attendant. The overall objective of this study is to determine the effect of provider type in the occurrence and management of serious childbirth related complications among postpartum women at the community level in Bungoma and Lugari Districts of Western Province, Kenya. The proposed study will employ a case control study design in which women with obstetric complication(s)will be cases and women without obstetric complications will be controls. Controls will be sampled concurrently with the cases. Each time a new case is diagnosed, a control is selected from the population at risk in the neighborhood at that point in time. The study population will consist of women aged 15-49 years with a delivery in the past 12 months. A woman who reports having experienced a birth-related complication will be recruited as a case while woman who reports having experienced no complication during child-birth will be recruited as a control.

NCT ID: NCT01664520 Completed - Clinical trials for Subarachnoid Hemorrhage

Dexmedetomidine and Subarachnoid Haemorrhage

Start date: June 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to investigate how dexmedetomidine affects static and dynamic autoregulation, intracranial pressure (ICP) and cerebral oxygenation in aneurysmal subarachnoid haemorrhage (SAH) patients.

NCT ID: NCT01662895 Terminated - Clinical trials for Intracerebral Hemorrhage

High-Dose Deferoxamine in Intracerebral Hemorrhage

HI-DEF
Start date: March 18, 2013
Phase: Phase 2
Study type: Interventional

The main purpose of this study is to determine whether treatment with deferoxamine mesylate is of sufficient promise to improve outcome before pursuing a larger clinical trial to examine its effectiveness as a treatment for brain hemorrhage.

NCT ID: NCT01659008 Recruiting - Clinical trials for Menstrual Cycle and Uterine Bleeding Disorders

Estradiol vs Lysteda in Treatment of Heavy Menstrual Bleeding

Start date: June 2012
Phase: N/A
Study type: Interventional

Treatment with Estradiol is non-inferior to treatment with Tranexamic acid in reducing the amount and duration of menstrual blood loss in women with cyclic heavy menstrual bleeding