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Hemorrhage clinical trials

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NCT ID: NCT04777097 Recruiting - Blood Loss Clinical Trials

Blood Loss and Preeclampsia

Start date: January 1, 2021
Phase:
Study type: Observational

Study of blood loss in preeclamptic patients using mathematical formulae

NCT ID: NCT04775836 Recruiting - Stroke Clinical Trials

An EHR-based Platform To Facilitate Outcomes and Research Methods in Cerebrovascular Diseases

PLATFORM-CVD
Start date: January 1, 2018
Phase:
Study type: Observational [Patient Registry]

In this protocol, the investigators present methods and preliminary results from the PLATFORM-CVD Study, an EHR-based multicenter cohort. This study will focus on assessing the distribution of major cerebrovascular diseases, determining the risk factors associated with disease incidence and worse in-hospital outcomes, as well as describing the quality of care. Data from this cohort will be used to develop suitable prediction models for cerebrovascular diseases using real-world data and to understand how outcomes for cerebrovascular diseases would change with quality improvement interventions.

NCT ID: NCT04773002 Completed - Hemorrhage Clinical Trials

A Comparison of Volatile Anesthesia and Total Intravenous Anesthesia (TIVA)

Start date: March 18, 2021
Phase:
Study type: Observational [Patient Registry]

In this study, investigators wanted to investigate the effect of volatile anesthesia and total intravenous anesthesia (TIVA) on ecchymosis, edema, and intraoperative bleeding in rhinoplasty.

NCT ID: NCT04771923 Completed - Bleeding Clinical Trials

Tranexamic Acid Versus Adrenaline for Controlling Iatrogenic Endobronchial Bleeding

TAVA
Start date: February 22, 2021
Phase: N/A
Study type: Interventional

Endobronchial bleeding is a relatively common complication of diagnostic bronchoscopy. Both tranexamic acid and adrenaline are used topically for the control of endobronchial bleeding. The aim of this study is to compare the efficacy of tranexamic acid with adrenaline in controlling iatrogenic endobronchial bleeding after diagnostic bronchoscopy.

NCT ID: NCT04771481 Completed - Effect of Drug Clinical Trials

Metoclopramide for Acute Upper GI Bleeding

Start date: April 10, 2021
Phase: Phase 4
Study type: Interventional

The presence of blood clot in stomach limited quality of endoscopic view ,which affect successful rate of hemostatic endoscopy in patient with acute upper gastrointestinal bleeding. The study is aimed to evaluate the efficacy of metoclopramide, as pro-kinetic agent ,for gastric visualization in the patient with acute UGIB; double-blind randomized controlled trial and two centers study. The patient were randomly assigned to receive either metoclopramide (10mg) intravenously or placebo before endoscopy 30-120 min. The primary endpoint was endoscopic yield, assessed by objective gastric visualized scoring systems. Secondary end points include duration of endoscope, technical success rate, the need for second-look EGD, units of blood transfusion, length of hospital stay and 30-day rebleeding rate.

NCT ID: NCT04768582 Recruiting - Clinical trials for Acute Coronary Syndrome

Platelet Reactivity After an Eastern Asian Loading Dose of Prasugrel in Taiwanese ACS Patients

PREP-TAMI
Start date: May 1, 2020
Phase: N/A
Study type: Interventional

Prasugrel has a faster onset of action and greater platelet inhibition with less inter-individual response variability than clopidogrel. Japan and Taiwan are the only two nations where adjusted/Asian dose of prasugrel (loading dose (LD)/maintenance (MD): 20/3.75 mg) was approved for clinical use. However, there is no data regarding the effectiveness of adjusted dose of prasugrel on platelet reactivity in Taiwanese patients with acute coronary syndrome (ACS). This study aim to evaluate the pharmacodynamic of the Asian dose prasugrel on the platelet reactivity after percutaneous coronary intervention (PCI) for patients with ACS.

NCT ID: NCT04760873 Suspended - Bleeding Clinical Trials

Cryotherapy for GAVE

GAVE Cryo
Start date: October 14, 2020
Phase: N/A
Study type: Interventional

Gastric antral vascular ectasia (GAVE) is a condition that can lead to blood loss in the gastrointestinal tract and low blood counts or anemia. 1,2 GAVE is commonly associated with liver disease, kidney disease and autoimmune immune problems, but can also be seen in patients without those problems. 2-4 It is common for GAVE to cause hospitalization of patients and significant blood transfusion requirements. Given these problems, effective treatment of GAVE is needed to reduce these potential problems. These treatments are performed by a gastroenterologist through a flexible endoscope most often with argon plasma coagulation (APC).5-7 APC is only partially successful at eradicating GAVE and often entails repeated endoscopic procedures. Therapy with APC can also cause ulceration at times resulting in acute bleeding. Cryoablation is an attractive alternative to APC as it should not cause increased blood loss and case reports suggest that ablation may be achieved with limited number of endoscopic sessions. Prior problems with endoscopic cryotherapy include the high flow of gas and risk of perforation.8,9 A recent retrospective investigation by this group has evaluated the first generation cryotherapy balloon, demonstrating clinical safety and efficacy for GAVE.10 A new balloon cryotherapy spray device was recently developed and does not require venting. In this study we plan to prospectively evaluate the use of balloon cryotherapy to treat GAVE. We predict that the therapeutic response of balloon cryotherapy will be greater than 80% effective at achieving clinical success or the loss of overt bleeding and need for packed red blood cell (PRBC) transfusion at 6 months after treatment.

NCT ID: NCT04760717 Recruiting - Ischemic Stroke Clinical Trials

Regulating Blood Pressure During Recovery From Intracerebral Hemorrhage and Ischemic Stroke

REDUCE
Start date: March 19, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this research study is to determine whether blood pressure treatment regimens with spironolactone are better than blood pressure treatment regimens without spironolactone at lowering blood pressure in stroke survivors.

NCT ID: NCT04760301 Recruiting - Blood Loss Clinical Trials

Local Tranexamic Acid During Vaginal Hysteractomy to Reduce Blood Loss

Start date: February 16, 2021
Phase: N/A
Study type: Interventional

Assessing the efficiency of Prophylactic use of local tranexamic acid during vaginal hysterectomy to reduce blood loss during operation

NCT ID: NCT04758377 Recruiting - Clinical trials for Traumatic Spinal Cord Haemorrhage

Characterizing Hemorrhage in Acute Spinal Cord Injury With MRI

CHASM
Start date: February 6, 2021
Phase: N/A
Study type: Interventional

The study is designed to determine whether hemorrhage within the injured spinal cord is influenced by mean arterial pressure (MAP) augmentation with vasopressors and by venous thromboembolism (VTE) prophylaxis with anticoagulants in the first two weeks following a traumatic spinal cord injury (tSCI).