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Hemorrhage clinical trials

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NCT ID: NCT03361124 Withdrawn - Clinical trials for Uterine Atony With Hemorrhage

Oxytocin Dosing at Planned Cesarean Section and Anemia

Start date: March 1, 2019
Phase: Phase 4
Study type: Interventional

Patient's with planned cesarean sections will be randomized to receive either standard 20 mU in 1L as a bolus following delivery of the placenta or 20 mu in 1L following delivery of the placenta plus an additional 20 mU in 1L over 8 hours.

NCT ID: NCT03340116 Withdrawn - Burns Clinical Trials

Measurement of Blood Volume Loss During Burn Surgery

Start date: January 2020
Phase:
Study type: Observational

Burn surgery is associated with significant reductions in hematocrit. However, it is unclear whether these reductions are the result of hemodilution from non-red cell containing intraoperative transfusions or from loss of red blood cells. The investigators will be using the Daxor Blood Volume Analyzer (BVA-100), an FDA approved instrument that can measure total blood volume, plasma volume, and RBC volume using the indicator dilution technique. By comparing pre-operative measurements of blood volume, plasma volume, and RBC volume to that of post-operative measurements after burn surgery, the investigators can determine the primary cause of the reduction in hematocrit associated with burn surgery. The investigators hypothesize that these reductions in hematocrit are primarily the result of hemodilution rather than blood loss and that there will be a statistically significant difference in measured plasma volume from the pre-operative group to the post-operative group.

NCT ID: NCT03326596 Withdrawn - Clinical trials for Postpartum Hemorrhage

Prevention of Postpartum Hemorrhage With TXA

TXA
Start date: April 20, 2018
Phase: Phase 4
Study type: Interventional

Hemorrhage remains the leading cause of maternal death worldwide. Tranexamic acid has been shown to reduce rates of hemorrhage when given prophylactically prior to cesarean delivery. It has also been shown to be an effective treatment in response to hemorrhage after a vaginal delivery. The aim of this study is to assess the impact of TXA on hemorrhage rates when given prophylactically prior to all deliveries.

NCT ID: NCT03325868 Withdrawn - Dysmenorrhea Clinical Trials

Effect of Ulipristal Acetate on Bleeding Patterns and Dysmenorrhea in Women With Adenomyosis

Start date: February 2018
Phase: Phase 4
Study type: Interventional

Adenomyosis affects approximately 21% of symptomatic women who present to gynecology clinics. The disease is characterized by heavy bleeding and pain during periods. Limited treatment options exist for the treatment of adenomyosis for women who desire future child-bearing or prefer to avoid surgery. Recently, ulipristal acetate has been studied as a treatment option for women who have fibroids and heavy bleeding. The majority of women treated with ulipristal stopped having periods altogether. Our study aims to determine whether ulipristal is an adequate treatment for women with adenomyosis.

NCT ID: NCT03303235 Withdrawn - Clinical trials for Postpartum Hemorrhage

Intravenous Versus Intramuscular Administration of Methylergonovine for Uterine Contraction in Cesarean Sections

Start date: July 2020
Phase: Early Phase 1
Study type: Interventional

Insufficient uterine tone resulting in atony can potentiate hemorrhage and adverse outcomes for the parturient. Oxytocin is the first pharmacologic agent used, followed by methylergonovine, carboprost, and misoprostol. The American Congress of Obstetricians and Gynecologists (ACOG) recommends the sequential use of oxytocin, followed by methylergonovine, carboprost, misoprostol, then surgical intervention for cases of refractory uterine atony. Many studies have examined the effect and dosage of intravenous uterotonics, including oxytocin. Although there are anecdotal reports of using intravenous bolus or rapid infusion of methylergonovine, no randomized trial has compared efficacy and side effects of these two routes of administration. Investigators hypothesize that intravenous methylergonovine reduces the time to adequate uterine tone (the tone at which the uterus is adequately contracted to prevent atony after delivery of neonate), decreases the total dose of methylergonovine to contract the uterus, and therefore produces fewer side effects of hypertension, nausea, and vomiting. Reducing the time to achieve adequate uterine tone is likely to decrease postpartum hemorrhage.

NCT ID: NCT03300479 Withdrawn - Clinical trials for Nontraumatic Intracerebral Hemorrhage, Multiple Localized

Clevidipine (Cleviprex®) Compared With Urapidil (Ebrantil®)

Clevidipine
Start date: June 15, 2017
Phase: Phase 4
Study type: Interventional

Intracerebral hemorrhage (ICH) is responsible for 10-15% of primary strokes. ICH is a dynamic process with three phases: initial hemorrhage, followed by hematoma expansion and perihematoma edema formation. Hematoma volume is correlated with disease progression and outcome. Contemporary evidence proposes that elevated blood pressure is associated with hematoma expansion while more than 90% of patients with ICH present with acute hypertension. Uncontrolled blood pressure is a leading cause of ICH and it seems also to be a factor of poorer outcomes. Therefore, rapid reduction and control of blood pressure might ease disease progression and improve the outcome. Clevidipine (Cleviprex®), an ultrashort-acting dihydropyridine calcium channel antagonist, with its rapid onset and short duration might be more effective than conventional antihypertensives to achieve rapid blood pressure control in patients with acute ICH.

NCT ID: NCT03125551 Withdrawn - Dietary Supplements Clinical Trials

ROTEM and Dietary Supplements

Start date: June 2017
Phase: N/A
Study type: Interventional

Dietary Supplements can affect platelet activation and aggregation, which could result in bleeding tendencies. This study wishes to evaluate the influence that these supplements has on platelet function using Rotational thromboelastometry.

NCT ID: NCT03027973 Withdrawn - Clinical trials for Heavy Menstrual Bleeding

Quality of Life Outcomes for Ulipristal Acetate and Tranexamic Acid in the Management of Heavy Menstrual Bleeding

Start date: January 2020
Phase: Phase 1
Study type: Interventional

This study compares two treatments for the management of heavy menstrual bleeding, ulipristal acetate (UPA) and tranexamic acid (TEA), on health-related quality of life. Half of the participants will receive UPA and a placebo, and the other half will receive TEA and a placebo.

NCT ID: NCT02946437 Withdrawn - Clinical trials for Subarachnoid Haemorrhage (SAH)

Sevoflurane in Subarachnoidal Haemorrhage

Sevoflurane
Start date: November 1, 2015
Phase: Phase 2
Study type: Interventional

Feasibility and safety of short term application of sevoflurane in patients with SAH treated with aneurysm coiling or clipping in the setting of a neurointensive care unit.

NCT ID: NCT02933840 Withdrawn - Hemorrhage Clinical Trials

Using a Remote Patient Monitoring Alert System to Improve Care

Start date: January 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the efficacy of a remote patient monitoring platform and alert system in reducing adverse events for hospitalized geriatric orthopedic trauma patients.