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Blood Loss, Surgical clinical trials

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NCT ID: NCT02733952 Recruiting - Clinical trials for Post Operative Hemorrhage

Intravenous Tranexamic Acid Versus Pericervical Tourniquet To Decrease Blood Loss In Trans-Abdominal Myomectomy

Start date: August 2015
Phase: Phase 3
Study type: Interventional

Intravenous Tranexamic Acid Versus Pericervical Tourniquet To Decrease Blood Loss In Trans-Abdominal Myomectomy

NCT ID: NCT02730533 Completed - Stomach Neoplasms Clinical Trials

The Efficacy of Esomeprazole Premedication on Intraoperative Bleeding During Gastric ESD

Start date: March 2016
Phase: N/A
Study type: Interventional

This will be a single-centre, randomised, endoscopist-blind, parallel-group study in patients who are scheduled endoscopic submucosal dissection (ESD) for gastric mucosal lesion. The primary objective is to observe whether a regimen of 7-day oral esomeprazole premedication can alleviate intraoperative bleeding in patients scheduled for ESD due to gastric mucosal lesions.

NCT ID: NCT02702128 Completed - Surgery Clinical Trials

Preventive EXACYL® on Perioperative Bleeding During Orthognathism of Maxillary Surgery

LEFORTEXACYL
Start date: January 3, 2016
Phase: Phase 3
Study type: Interventional

Prospective, randomized, double-blind, placebo-controlled, mono center, Phase III trial to compare EXACYL in preventive with placebo on perioperatory bleeding in orthognathism surgery.

NCT ID: NCT02674906 Completed - Clinical trials for Intra Operative Bleeding, Blood Salvage

Exposure of Salvaged Blood to Inflammation and Oxidative Stress: the Effect of Different Anticoagulant Regimes (HECICS)

HECICS
Start date: February 2016
Phase: N/A
Study type: Interventional

The primary aim of this randomized controlled study is to determine whether the use Anticoagulant Citrate Dextrose Solution--Formula A (ACD-A) in cell salvage reduces inflammation and oxidative stress in cell saver blood compared to heparin. The secondary aim is to determine whether any differences in activation can be correlated to any differences in postoperative clinical outcome.

NCT ID: NCT02631889 Not yet recruiting - Clinical trials for Blood Loss, Surgical

Study to Assess the Effectiveness of Transcollation Technology to Reduce Bleeding in Lung Surgery

Start date: March 2016
Phase: N/A
Study type: Interventional

Major lung resection is one of the most common procedures performed in thoracic surgery, but it may involve considerable bleeding and the occasional need for a transfusion and/or reoperation for bleeding in specific cases. In addition, lysis of pleural-parenchymal adhesions and dissection can represent a challenge in patients who have undergone chemotherapy and/or radiation therapy, and in patients with bronchiectasis or COPD. Several intraoperative methods have been used to manage blood loss, including topical haemostatic agents, bipolar sealers or electrocautery. Transcollation technology (TT) consists of a disposable bipolar sealer that uses a radiofrequency coagulation system to deliver a saline solution that provides haemostatic sealing of soft tissue and bone and provides localized cooling without charring. Blood loss reduction has been previously described in several fields of surgery. The primary end-point of the proposed trial is to assess if the ability of Transcollation Technology in reducing the proportion of patients showing bleeding perioperatively within the setting of a prospective randomized controlled trial. The secondary end-point is to assess if Transcollation Technology is able to improve postoperative outcomes reducing the length of hospital stay.

NCT ID: NCT02588716 Completed - Clinical trials for Hepatectomy, Surgical Blood Loss, Terlipressin

Effects of Terlipressin on Blood Loss and Transfusion Requirements During Major Liver Resection.

Start date: September 2015
Phase: Phase 2
Study type: Interventional

To evaluate the effects of Terlipressin infusion on blood loss & transfusion requirements in cirrhotic patients undergoing major liver resections.

NCT ID: NCT02580227 Recruiting - Hip Fractures Clinical Trials

Tranexamic Acid in Intertrochanteric and Subtrochanteric Femur Fractures

Start date: June 2015
Phase: Phase 4
Study type: Interventional

The objective of this study is to evaluate the effect of Tranexamic Acid (TXA) on blood loss and need for perioperative blood transfusion following intertrochanteric and subtrochanteric femur fractures. TXA is a antifibrinolytic medication that prevents the breakdown of blood clots by inhibiting the activation of plasminogen to plasmin in the coagulation cascade. Our hypothesis is that by providing TXA at the time of hospital admission it will decrease the amount of preoperative and intraoperative bleeding thereby leading to a decreased need for post-operative transfusion. This a double blinded, placebo controlled, therapeutic trial in which half of patients will be randomized to receive TXA at the time of hospital admission and half of patients will receive a placebo.

NCT ID: NCT02557672 Completed - Bleeding Clinical Trials

PCC vs. FFP for Post Cardiopulmonary Bypass Coagulopathy and Bleeding

Start date: August 2016
Phase: Phase 4
Study type: Interventional

This will be the first prospective randomized controlled clinical trial directly comparing Prothrombin Complex Concentrate (PCC) Compared to Fresh Frozen Plasma (FFP) for post cardiopulmonary bypass microvascular bleeding and factor-mediated coagulopathy. Is there a difference in bleeding and transfusion requirements in patients received PCC versus FFP?

NCT ID: NCT02461329 Not yet recruiting - Clinical trials for Hemorrhage, Surgical

Comparison of the Effects of Gelatine Versus Balanced Crystalloid Solution for Volume Therapy

Gelaring
Start date: May 2015
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether volume therapy with a solution of gelatine has negative impact on coagulation, platelet function, renal function in comparison with crystaloid solution (Ringerfundin).

NCT ID: NCT02441751 Recruiting - Clinical trials for Blood Loss, Surgical

Intraoperative Volume Management and QT Interval

Start date: May 2015
Phase:
Study type: Observational

QT interval changes is measured during all phases of the operation. The protocol is focusing at intraoperative bleeding events and is also observing QT interval changes during anesthetic and operative procedures.