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Hemorrhage clinical trials

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NCT ID: NCT04396483 Recruiting - Contraception Clinical Trials

Dysfunctional Uterine Bleeding After Tubal Sterilization

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

In this study, the investigators will compare the frequency and amount of bleeding after tubal sterilization and salpingectomy

NCT ID: NCT04395963 Completed - Clinical trials for Simulation of Physical Illness

Eye Tracking and Simulated Postpartum Hemorrhage

Start date: November 20, 2019
Phase:
Study type: Observational

Eye tracking is the process of measuring an individual's eye movements in order to reflect their attentional behavior by using a device called an eye- tracker. This study uses eye-tracking methodology to observe the gaze patterns of participants to a high fidelity simulation scenario of postpartum hemorrhage acting in the role of leader to evaluate the relationship between eye-tracking patterns and leadership and team behavioral and technical skills.

NCT ID: NCT04394663 Recruiting - GI Bleeding Clinical Trials

High Dose Oral Omeprazole in High Risk UGIB

Start date: October 1, 2020
Phase: N/A
Study type: Interventional

Peptic ulcer bleeding is the most common etiology in upper gastrointestinal bleeding all over the world. After endoscopic treatment, proton pump inhibitor (PPI) is recommended to prevent re-bleeding. Intravenous PPI is recommended as a standard treatment.In the past, there were many trials showing the efficacy of high-dose oral PPI after endoscopic hemostasis but most were industrial sponsor which assessing an expensive PPI. Moreover, the number of patients in those studies were insufficient to confirm a non-inferiority outcome in term of rebleeding by using oral PPI. This study will evaluate a high-dose, local-made PPI (omeprazole) in peptic ulcer treatment after successful endoscopic hemostasis compared to standard IV PPI continuous drip.

NCT ID: NCT04394234 Completed - Uterine Hemorrhage Clinical Trials

A Study of Severe Uterine Bleeding Following Exposure to Direct Oral Anticoagulants

Start date: May 15, 2020
Phase:
Study type: Observational

The purpose of this study is assess the: (a) incidence of severe uterine bleeding (SUB) following exposure to individual direct oral anticoagulant (DOACs) (rivaroxaban, apixaban, dabigatran) and warfarin, (b) individual DOACs (rivaroxaban, apixaban, dabigatran) association with risk of SUB compared with warfarin, and (c) individual DOACs (rivaroxaban, apixaban, dabigatran) associated with risk of SUB compared with other individual DOACs - among women with prior diagnoses for DOAC and warfarin indications (non-valvular atrial fibrillation [NVAF], venous thromboembolism [VTE], total hip replacement [THR] or total knee replacement [TKR]).

NCT ID: NCT04388917 Completed - Kidney Cancer Clinical Trials

Does the Use of Hemostatic Clips During the Tumor Resection Step Reduce Blood Loss During Robot-assisted Partial Nephrectomy?

Start date: January 1, 2017
Phase:
Study type: Observational

One challenge of robot-assisted partial nephrectomy (RAPN) is to reduce operative blood loss. Partial nephrectomy (PN) is a complex surgery that is being made easier by robotic assistance. In this study, we determined whether the use of hemostatic clips during the tumor resection step reduced blood loss during robot-assisted partial nephrectomy. Methods: In this retrospective study, we included all consecutive patients who underwent RAPN in our university hospital from 2017 to 2019. Three experienced surgeons performed the surgery. One surgeon used Hemo-lock hemostatic clips during tumor resection to prevent bleeding, and two did not. Blood loss in the two groups was compared as the primary endpoint. The duration of clamping, operative time, complications, surgical margins, transfusions, serum creatinine and hemoglobin were compared as secondary endpoints. Results: 53 patients were included, 36 in the No-clip group and 17 in the Clip group. Our two groups were comparable for age, weight, Charlson score, tumor size and RENAL score. There was a significant difference between the two groups for median blood loss 50 mL in the Clip group versus 300 mL in the No-clip group (p = 0.0001), whereas median operating time was shorter in the No-clip group, 140 min versus 180 min for the Clip group (p = 0.044). No other criterion showed a significant difference. The use of Hemo-lock during the tumor resection step in RAPN reduced blood loss without impairing renal function. Larger studies are still needed to confirm our findings.

NCT ID: NCT04388722 Withdrawn - Hypovolemia Clinical Trials

Monitoring Noninvasively for Infusion and Transfusion Optimization

Start date: June 1, 2020
Phase: N/A
Study type: Interventional

This is a multicenter, cluster randomized controlled trial to assess the effects of an optimized intraoperative fluid and blood management strategy on postoperative complications.

NCT ID: NCT04387305 Not yet recruiting - Hemorrhage Clinical Trials

Traumatic Injury Clinical Trial Evaluating Tranexamic Acid in Children: An Efficacy Study

TIC-TOC
Start date: October 1, 2024
Phase: Phase 3
Study type: Interventional

Trauma is the leading cause of death and disability in children in the United States. The objective of this study is to evaluate the benefits and harms of tranexamic acid (TXA; a drug that stops bleeding) in severely injured children with hemorrhagic brain and/or torso injuries. Using thromboelastography, we will measure baseline fibrinolysis to assess for treatment effects of TXA at different levels of fibrinolysis.

NCT ID: NCT04386642 Not yet recruiting - Meningioma Clinical Trials

Tranexamic Acid Reduce Blood Loss in Meningioma Resection

Start date: September 1, 2021
Phase: Phase 4
Study type: Interventional

In neurosurgical setting, a large sample size trials of tranexamic acid (TXA) has been limited to TBI and SAH. The evidence of TXA in brain tumor was scarce. A few case reports support the role of TXA in brain tumor patients with significant intraoperative bleeding and difficult achieving hemostasis. To prove the benefit of TXA for an attenuation of blood loss in brain tumor patients, research with a larger sample size is required. This prospective, randomized double-blind controlled study will be conducted to evaluate the effect of TXA in reducing blood loss and blood transfusion in patients with intracranial meningiomas, diameter > 5 cm in at least 2 dimensions from the latest radiographic findings.

NCT ID: NCT04385953 Completed - Trauma Clinical Trials

QStat in Trauma and Obstetric Hemorrhage

Start date: December 10, 2019
Phase:
Study type: Observational

This study will evaluate the performance of the Quantra System comprised of the Quantra Hemostasis Analyzer with the QStat Cartridge in trauma patients and obstetric patients with postpartum hemorrhage.

NCT ID: NCT04381416 Completed - Clinical trials for Abnormal Uterine Bleeding

Study to Assess the Safety and Efficacy of the IUB SEADâ„¢ Device

AUB
Start date: September 1, 2019
Phase: N/A
Study type: Interventional

Pre-pivotal, randomized study to assess the safety and efficacy of the IUB SEADâ„¢ device in women suffering from abnormal uterine bleeding.