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Blood Loss, Surgical clinical trials

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NCT ID: NCT00285623 Completed - Clinical trials for Blood Loss, Surgical

Observational Cohort Study of TachoSil (TC-018-IN)

Start date: December 2005
Phase: Phase 4
Study type: Observational

The purpose of this study is to collect information, after exposure to TachoSil ®, of all thromboembolic events, immunological events and drug interactions leading to thromboembolic events or major bleeding. In addition, pharmacoeconomic data will be collected.

NCT ID: NCT00279383 Completed - Clinical trials for Blood Loss, Surgical

OSHES - Observational Study on Hemostasis in Surgery (TC-022-IT)

Start date: August 2005
Phase: Phase 4
Study type: Observational

OSHES (= Observational Study on Hemostasis in Surgery) is a non interventional register settled in Italy with the purpose of collecting data on 800 patients intra-operatively treated with hemostatic supporting agents/techniques in addition to the standard surgical procedures in 40 surgical wards. The availability of these data will allow for a better understanding of the therapeutic needs in the area of hemostatic supporting agents/techniques.

NCT ID: NCT00264095 Completed - Neoplasms Clinical Trials

An Observational Study of Blood Management Techniques in Oncology Surgical Treatment

Start date: July 2004
Phase: Phase 4
Study type: Observational

The purpose of this study is to observe the methods used to manage blood loss in surgical procedures to remove tumors from patients with cancer and to determine if there is a relationship with the need for blood transfusions.

NCT ID: NCT00221741 Completed - Clinical trials for Blood Loss, Surgical

Fresh Frozen Plasma in Cardiac Surgery: Descriptive and Prognostic Study

PLASMACARD
Start date: February 2004
Phase: N/A
Study type: Observational

Despite experts' recommendations, the consumption of Fresh frozen plasma (FFP) is very heterogeneous among French cardiac surgery centers. This probably reflects heterogeneous practices that are not characterized and whose outcomes on morbidity and mortality are not documented. The principal objective of the study is to describe transfusional strategies of FFP in patients undergoing cardiac surgery. The other objectives are: to assess the conformity of FFP transfusion or lack of transfusion to current French authorities' recommendations, to describe the post-operative mortality and morbidity and to assess the prognostic role of FFP on mortality and morbidity. Prognostic analyses will take into account other prognostic factors of mortality and morbidity. 1500 patients undergoing cardiac surgery and presenting with a serious bleeding (or transfused with FFP without bleeding) will be included in the study.