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Blood Loss clinical trials

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NCT ID: NCT01881568 Completed - Blood Loss Clinical Trials

Efficacy Comparison of Topical and Intravenous Tranexamic Acid to Reduce the Number of Blood Transfusions in TKA

TRANEX1
Start date: January 2013
Phase: Phase 3
Study type: Interventional

The main objective is to evaluate the efficacy and safety of topical Tranexamic Acid (TA) to reduce the blood transfusion rate in total knee arthroplasty. The secondary endpoints are to estimate the visible blood loss at 24 hours after surgery, and invisible blood loss through serial counting of Hb/Htc. Methodology. TRANEX1 is a phase III, unicentric, controlled, randomized, double blind clinical trial that compare efficacy and safety of topical TA versus intravenous TA in a multimodal protocol, with no-inferiority criteria(n=79).

NCT ID: NCT01846195 Completed - Blood Loss Clinical Trials

Evaluation of the Zynex Blood Volume Monitor in Healthy Adult Patients During a Blood Draw

Start date: June 6, 2012
Phase: N/A
Study type: Interventional

Non-invasive monitoring to measure changes in blood volume.

NCT ID: NCT01834612 Completed - Blood Loss Clinical Trials

Evaluation of the Zynex Blood Volume Monitor in Healthy Adult Volunteers During a Blood Draw

Start date: January 7, 2013
Phase: Phase 1
Study type: Interventional

To determine if a manual blood loss can be detected using the non-invasive blood monitor.

NCT ID: NCT01793987 Not yet recruiting - Blood Loss Clinical Trials

Coblation in Endoscopic Sinus Surgery

Start date: May 2013
Phase: N/A
Study type: Interventional

Chronic Rhinosinusitis (CRS) refers to a pathological condition where the sinonasal mucosa is inflamed for greater than 12 weeks(1). It is associated with a constellation of symptoms, including facial pain, anosmia, and nasal congestion. It has been estimated that CRS affects close to 5% of the Canadian population(2). When medical therapy fails, patients are often referred to Otolaryngology- Head and Neck Surgeons for consideration of surgical management. Endoscopic sinus surgery (ESS) is one of the mainstays of therapy for CRS that has failed medical management(3). Traditionally, the microdebrider has been the go-to tool for performing these surgeries, but recently the Coblator (ArthroCare, Austin, Texas) has begun to define its' role in surgery. By using bipolar radiofrequency energy to ablate tissue (with temperatures up to 60˚ C)(4), theoretically the Coblator will result in less bleeding than so-called "cold" surgical techniques (i.e. the microdebrider). In a retrospective study by Eloy et. al, patients with CRS and nasal polyposis had a statistically significant amount of less intraoperative blood loss when the Coblator was used in their surgery, than those patients who underwent surgery with the microdebrider. The investigators plan to further investigate this in a randomized, controlled fashion

NCT ID: NCT01712971 Withdrawn - Surgery Clinical Trials

Reduced Intra-operative Blood Loss in Pancreaticoduodenectomy for Pancreatic or Peri-ampullary Tumors; Monocentric Trial on Standard Open Versus Minimally Invasive Surgery

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

The incidence of complications after standard open pancreaticoduodenectomy for pancreatic or peri-ampullary tumours is around 50%. The amount of intra-operative blood loss is an important factor that determines the occurrence of postoperative complications. Therefore, any significant reduction of intra-operative blood loss will benefit the peri-operative course.

NCT ID: NCT01646060 Completed - Healthy Clinical Trials

Clinical Evaluation of the Zynex Blood Volume Monitor (CM-1500) in Healthy Male Adult Subjects During a Blood Draw

Start date: November 2011
Phase: Phase 1
Study type: Interventional

Zynex's blood volume monitor (BVM) is a non-invasive monitoring device to monitor blood volume and blood loss of a patient during surgery, post operatively and/or in recovery. This monitoring device will identify baseline blood volume and relative changes in blood volume using a specific algorithm to compare and review data already monitored during surgery, displaying blood volume and blood loss in real-time.

NCT ID: NCT01608386 Enrolling by invitation - Blood Loss Clinical Trials

A Study of Anterior Approach Combined With Infrahepatic Inferior Vena Cava Clamping

AA+IVC
Start date: May 2012
Phase: N/A
Study type: Interventional

Anterior approach results in better operative and survival outcomes compared with the conventional approach in patients with large hepatocellular carcinoma (HCC), but anterior approach has the problem of bleeding from the hepatic vein. Our previous study showed that infrahepatic inferior vena cava (IVC) clamping can reduce blood loss during conventional hepatic resection. The investigators guess infrahepatic IVC clamping may also reduce blood loss in anterior approach right hepatic resection. So the investigators conduct this prospective, randomized, controlled trial to compare anterior approach combined with infrahepatic IVC clamping and anterior approach in major right hepatectomy for large HCC.

NCT ID: NCT01604668 Completed - Blood Loss Clinical Trials

Comparative Accuracy of Three Versions of Non-Invasive Hemoglobin Monitoring

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

There is no study hypothesis. The purpose of this study is to compare the accuracy of the: 1) SpHb (Radical 7 Pulse Co-Oximetry with SpHb™) RevF sensor (currently marketed), 2) the SpHb RevG sensor (a new, limited release version), and 3) the Pronto-7 sensor (currently marketed version) in patients undergoing spine surgery.

NCT ID: NCT01594671 Completed - Blood Loss Clinical Trials

Tranexamic Acid for Unilateral Total Knee Arthroplasty

TRANEXTOP
Start date: February 2012
Phase: Phase 3
Study type: Interventional

Total knee arthroplasty is often associated with excessive postoperative bleeding due to increased fibrinolysis. Hence, the objective of the proposed of this multicentre study is to determine the peri-operative bleeding comparing the application of topical and intravenous tranexamic acid with the habitual surgical haemostasis.

NCT ID: NCT01563380 Completed - Pain Clinical Trials

Role of Autologous Platelet Rich Plasma in Total Knee Arthroplasty

PRPTKA2012
Start date: January 2010
Phase: N/A
Study type: Interventional

This study was designed to evaluate the efficacy of leucocyte free autologous platelet rich plasma on blood loss, pain, wound healing and functional outcome after total knee arthroplasty. The investigators hypothesized that application of platelet rich plasma would help in reducing blood loss, postoperative pain and expedite wound healing and better short-term functional outcome following total knee arthroplasty.