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Hemorrhage clinical trials

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NCT ID: NCT02716532 Completed - Clinical trials for Subarachnoid Hemorrhage, Aneurysmal

Bioavailability of Medium Chain Triglycerides (MCTs) in Comatose Patients With Acute Brain Injury (ABI)

MCTs and ABI
Start date: April 2016
Phase: N/A
Study type: Interventional

This study will be targeting patients suffering from acute brain injury (ABI), including those with severe trauma brain injury (sTBI) and those with aneurysmal sub arachnoid hemorrhage (aSAH). This clinical study is an open-label, non-randomized, single-center, exploratory metabolic study. The primary objective is to determine changes from baseline (before enteral administration of Peptamen AF) in plasma and brain extracellular levels of MCFAs and Ketone bodies in sTBI patients upon Peptamen AF nutritional support.

NCT ID: NCT02716142 Completed - Clinical trials for Bleeding During Myomectomy

Rectal Misoprostol Versus Sublingual Misoprostol Prior to Myomectomy

RM-SLM
Start date: March 1, 2017
Phase: Phase 4
Study type: Interventional

the aim of the study is To compare the effectiveness of rectally administered prostaglandin E1 synthetic analogue (misoprostol) 400 microgram versus sublingually administered misoprostol before myomectomy to decrease blood loss during and after the operation.

NCT ID: NCT02712879 Completed - Heart Surgery Clinical Trials

Moderate Bleeding in Cardiac Surgery Post Operative

SPO
Start date: March 11, 2016
Phase:
Study type: Observational

Determine a bleeding threshold by measuring the blood volume in ml / kg / h collected in the drainage system to define moderate bleeding postoperative cardiac surgery and define the population.

NCT ID: NCT02712788 Terminated - Cerebral Vasospasm Clinical Trials

Milrinone in Addition to Hyperdynamic Therapy in the Treatment of Vasospasm Following Aneurysmal Subarachnoid Hemorrhage

Start date: April 18, 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the usefulness of adding Milrinone to the current standard treatment for cerebral vasospasm.

NCT ID: NCT02709564 Completed - Clinical trials for Blood Loss in Myomectomy

Sublingual Misoprostol in Decreasing Blood Loss Prior to Myomectomy

SL-MISO
Start date: December 2016
Phase: Phase 3
Study type: Interventional

The aim of the study is to compare the effectiveness of sublingual administered prostaglandin E1 synthetic analogue (misoprostol) 400 microgram versus placebo before myomectomy to decrease blood loss during and after the operation.

NCT ID: NCT02709460 Recruiting - Clinical trials for Postoperative Hemorrhage

Lateral Occlusion of Uterine Artery in Total Laparoscopic Hysterectomy

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

Laparoscopic hysterectomy is associated with complications in form of infections and subsequently dehiscence of the vault. This is a serious complication. The infection may be related to the frequently observed postoperative hematoma following traditional laparoscopic hysterectomy where the uterine artery is coagulated and divided at the cervical entry into the uterus. By coagulation of the uterine artery laterally close to the internal iliac artery this problem may be eliminated due to the much less bleeding observed during this procedure.

NCT ID: NCT02707484 Completed - Clinical trials for Gastrointestinal Vascular Malformation

the Efficiency of Thalidomide for Recurrent Small Intestinal Bleeding Due to Gastrointestinal Vascular Malformation

Start date: April 2016
Phase: Phase 3
Study type: Interventional

Gastrointestinal vascular malformation (GIVM), which is an important cause of acute or chronic gastrointestinal bleeding, currently lacks of effective treatment. The investigators' previous study first confirmed thalidomide treatment of GIVM bleeding was safe and effective. This prospective multi-center randomized controlled clinical trial intends to investigate the efficacy of thalidomide to the recurrent small intestinal hemorrhage due to GIVM.

NCT ID: NCT02705222 Completed - Uterine Bleeding Clinical Trials

Comparison Between D&C and Hysteroscopy in Management of AUB in Perimenopausal Women

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

The aim of this study is to compare dilatation and curettage with hysteroscopy in obtaining an accurate diagnosis of the etiology of abnormal uterine bleeding and outlining a mode of treatment-specific to the cause.

NCT ID: NCT02704780 Completed - Clinical trials for Postpartum Haemorrhage

Two Different Regimens of Misoprostol in Retained Placenta

Start date: March 2016
Phase: Phase 2
Study type: Interventional

This study evaluates intra umbilical vein injection of 800 µg versus 400 µg misoprostol for the treatment of retained placenta to reduce the need of manual removal of placenta under general anaesthesia

NCT ID: NCT02704637 Unknown status - Clinical trials for Subarachnoid Hemorrhage

An Evaluation of Non-invasive Acoustic Approach to Detect and Monitor Cerebral Vasospasm

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

HeadSense (HS)-1000 device, a proprietary non-invasive brain monitor, is expected to safely and accurately monitor physiological signs of the brain with minimal discomfort to patients, providing information about normal or abnormal brain-related conditions and providing decision-making support for physicians. The investigators hypothesize that the HS-1000 is capable of detecting vasospasm using the raw acoustic data derived from the noninvasive procedure.