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Blood Loss clinical trials

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NCT ID: NCT02403596 Completed - Clinical trials for Blood Loss After a Total Hip Replacement

Blood-sparing During Hip Prosthesis Surgery With Exacyl® in Patients Treated With Rivaroxaban

ESPER
Start date: October 20, 2015
Phase: Phase 3
Study type: Interventional

This study evaluates the efficacy of tranexamic acid versus placebo on perioperative blood loss using two dosage regimens (standard and extended) after a surgery during total hip arthroplasty in patients receiving the novel fast-acting oral anticoagulant rivaroxaban for prophylaxis of thrombosis.

NCT ID: NCT02374398 Completed - Blood Loss Clinical Trials

Clinical Trial Comparing Tranexamic Acid (TXA) With Aquamantys Sealer in Total Knee Arthroplasty (TKA)

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

The aim of the study is to determine if the use of iv TXA or Aquamantys system improve the postoperative hemoglobin and hematocrit after primary TKA and what is the effect of the simultaneous use of iv TXA and Aquamantys on the postoperative hemoglobin and hematocrit. The assumption is that the combination of iv TXA and Aquamantys system will enable an improvement in the postoperative hemoglobin and hematocrit equal or larger than the improvement generated by the use of Aquamantys system alone.

NCT ID: NCT02312440 Completed - Blood Loss Clinical Trials

Comparison of Topical and Intravenous Tranexamic Acid in Total Hip Arthroplasty

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

Recently, there has been interest in applying tranexamic acid topically before the closure of surgical wounds in total hip replacement. It has the advantages of ease of application, maximum concentration at the site of bleeding, minimising its systematic absorption and, potentially , decline the risks for systematic side-effects 。

NCT ID: NCT02311309 Completed - Surgery Clinical Trials

Epidemiology of Severe Peroperative Bleeding During Scheduled Surgery

Start date: November 2013
Phase: N/A
Study type: Observational

Peroperative bleeding has been studied in specific populations exposed to bleeding (i.e. cardiac surgery, orthopedic surgery). Epidemiology of peroperative bleeding and transfusion remain poorly studied in the whole cohort of patients scheduled for surgery remain unknown. The investigators conducted a prospective study in order to examine the incidence, and risk factors associated with peroperative bleeding and transfusion.

NCT ID: NCT02297061 Completed - Hip Fracture Clinical Trials

Can Thrombelastography Predict Blood Loss in Patients With Hip Fractures

Start date: December 2013
Phase: N/A
Study type: Observational

Hip fractures are associated with a large hidden blood loss. That is, the total blood loss associated with hip fracture surgery is much greater than that observed intra operatively. There is currently no viable method of identifying patients at risk of transfusion. The on admission haemoglobin level has been shown to be falsely reassuring . We are conducting a study of 200 consecutive hip fracture patients. Thrombelastography (TEG) is taken on admission. The results are blinded to clinicians. Results will be evaluated at the end of the study, comparing intra-operative and total blood losses with the TEG profile of the patient.

NCT ID: NCT02265562 Recruiting - Blood Loss Clinical Trials

Rectal Misoprostol and Blood Loss During Abdominal Hysterectomy

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

Hysterectomy, as any major operation, can cause complications, as hemorrhage which may occur in some cases and sometimes requiring blood transfusion. Recent study proved that misoprostol success in reducing blood loss during total abdominal hysterectomy when used once before the surgery.

NCT ID: NCT02233101 Completed - Clinical trials for Need for Blood Transfusion After Total Joint Arthroplasty

Oral vs. Intravenous TXA Study Proposal: TJA

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

Purpose: Examine oral and intravenous Tranexamic Acid (TXA) to determine whether or not the different routes of drug administration are equivalent in terms of post-operative reduction in hemoglobin, number of transfusions, and post-operative blood loss following TJA surgery. Hypothesis: Oral and intravenous TXA are equivalent routes of drug administration.

NCT ID: NCT02214524 Not yet recruiting - Hypothermia Clinical Trials

Comparison of Active and Passive Perioperative Warming Techniques in Reducing Intraoperative Blood Loss

Start date: August 2014
Phase: N/A
Study type: Interventional

This is a randomized, open label, parallel two arm, clinical study, which compare the Bair Hugger forced-air warming blanket and the conventional warming care practice in China on patients undergoing major surgery to determine the impact of maintaining normothermia on intraoperative blood loss, requirement for transfusion of packed red blood cells and the changes of coagulation function.

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: 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.