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Blood Loss clinical trials

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NCT ID: NCT01472913 Completed - Blood Loss Clinical Trials

Fibrin Sealant in Bilateral Simultaneous Total Knee Arthroplasty With Focus on Blood Loss, Pain, Swelling and Strength

Start date: August 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to measure the effect of fibrin sealant on reducing blood loss, pain and swelling when operated for bilateral total knee arthroplasty. Likewise the effect on Range Of Movement (ROM) and strength is examined.

NCT ID: NCT01436266 Terminated - Blood Loss Clinical Trials

Effect of Preoperative Buccal Misoprostol on Blood Loss in Second-trimester Dilation and Evacuation Abortion

Preop Miso
Start date: July 2011
Phase: Phase 3
Study type: Interventional

Misoprostol is a medication used extensively in obstetrics and gynecology for its ability to aid in softening the cervix as well as decreasing blood loss after abortion or vaginal delivery. Opinions vary as to its usefulness in aiding in cervical dilation, and in decreasing blood loss. The investigators propose to conduct a randomized, placebo-controlled trial to evaluate whether misoprostol given buccally 2 hours prior to second trimester surgical abortion decreases blood loss from the procedure. The investigators will also assess whether misoprostol improves cervical dilation, changes the length of the procedure, changes the need for additional mechanical dilation, changes the subjective ease of the procedure, and changes a woman's pain.

NCT ID: NCT01331499 Terminated - Blood Loss Clinical Trials

Salient Aquamantys Spine Trial

Start date: April 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare standard of care hemostasis techniques with and without the use of Aquamantys in reducing peri-operative blood loss.

NCT ID: NCT01099475 Completed - Blood Loss Clinical Trials

Effect of Intermittent Pedicle Clamping on Hepatocellular Injury During Liver Surgery

Start date: October 2007
Phase: N/A
Study type: Interventional

In order to prevent excessive blood loss during liver surgery, an intermittent Pringle manoeuvre (IPM) can be applied. This implies a temporary clamping of the portal vein and hepatic artery in the hepatoduodenal ligament in order to occlude hepatic inflow. The optimal duration of the IPM is unknown. This randomized controlled trial aimed to analyse differences in hepatocellular damage after 15 minutes or 30 minutes IPM during liver surgery for primary or secondary liver tumours.

NCT ID: NCT01048658 Completed - Anesthesia Clinical Trials

Sevoflurane as an Anesthetic During Dilation and Evacuation Procedures

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

Sevoflurane is an FDA-approved anesthetic drug commonly used for anesthesia during second trimester abortion procedures. It has a few advantages, including ease of use by the anesthesia provider. However, the literature suggests that when used in doses higher than those used at Oregon Health & Science University (OHSU) and Lovejoy, it is associated with an increase in the risk of bleeding. The investigators study aims to test whether the lower dose used at OHSU and Lovejoy during second trimester abortion procedures causes any difference in blood loss, when compared to similar abortion procedures for which this drug is not used.

NCT ID: NCT01038557 Completed - Anemia Clinical Trials

Frozen Red Blood Cell Transfusions in Trauma Patients

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

The purpose of this study is to look at red blood cell (RBC) transfusions in trauma patients and evaluate for any differences between the age of the RBCs and how they were stored. The investigators will specifically look for the following differences between study groups: 1. the transfused red blood cells' ability to delivery oxygen to the tissues 2. differences in biochemical markers in subjects and units transfused, and 3. how the subject's internal organs are working and if they develop any infections

NCT ID: NCT01014728 Completed - Blood Loss Clinical Trials

Intraoperative Bleeding During Endoscopic Sinus Surgery

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

The purpose of this study is to compare the blood loss during sinus surgery looking at two different types of anesthesia: either intravenous anesthesia with propofol or inhalational anesthesia with sevoflurane.

NCT ID: NCT00998647 Completed - Blood Loss Clinical Trials

Modified Ultrafiltration in Cardiac Surgery

Start date: June 2009
Phase: N/A
Study type: Observational

The purpose of this study is to find out, whether filtration of the blood in patients undergoing cardiac surgery, beneficially influences the coagulation system.

NCT ID: NCT00994994 Completed - Clinical trials for Congenital Heart Disease

Tranexamic Acid in Pediatric Cardiac Surgery

TXA
Start date: January 2006
Phase: N/A
Study type: Interventional

Tranexamic acid(TXA) is an antifibrinolytic agent to reduce blood loss in cardiac surgery. Previous seven RCTs comparing effects of TXA in pediatric cardiac surgery showed conflict results. The reason why they showed mixed results would be the imbalance of patients population with regard to presence of cyanosis. TXA would reduce blood loss in pediatric cardiac surgery with well balanced patients population.

NCT ID: NCT00990288 Completed - Blood Loss Clinical Trials

The Use of FLOSEAL to Reduce Bleeding in Total Knee Replacement Surgery

Start date: October 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if the agent, Floseal, can decrease the amount of blood patients lose after total knee replacement (TKR) surgery. If this product can be found to have an effect on bleeding, it may potentially reduce the problems associated with bleeding after knee replacement surgery such as pain, stiffness, and the need to have a blood transfusion. The subject's overall participation will be over a period of 6 weeks.