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Hemorrhage clinical trials

View clinical trials related to Hemorrhage.

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NCT ID: NCT02481011 Completed - Stroke Clinical Trials

Risk of Intracranial Hemorrhage in Users of Oral Antithrombotic Drugs

RICH
Start date: May 2015
Phase:
Study type: Observational

The true incidence and risks of intracranial hemorrhage (ICH) in patients on various antithrombotic treatments remain unknown. Here a nationwide study is conducted to investigate the risk for and incidence rates of ICH in users and non-users of various oral antithrombotic drugs in Norway between 2008 through 2014. Hopefully, this study will contribute to a more responsible prescription pattern of antithrombotic medications.

NCT ID: NCT02480556 Completed - Haemorrhage Clinical Trials

Comparing Blood Loss During Caesarean Section Between Manual Separation of Placenta & Conservative Management

Start date: July 2015
Phase: N/A
Study type: Interventional

to compare the blood loss during caesarean section between two different methods of separating the placenta after fetal extraction, keeping in mind that most blood loss occurs after placental separation.

NCT ID: NCT02478177 Completed - Stroke Clinical Trials

Addressing Real-world Anticoagulant Management Issues in Stroke

ARAMIS
Start date: September 2015
Phase:
Study type: Observational [Patient Registry]

The Addressing Real-world Anticoagulant Management Issues in Stroke (ARAMIS) registry is designed to provide important and timely insight into the management of acute stroke patients who are on novel oral anticoagulants in community practice.

NCT ID: NCT02475356 Completed - Clinical trials for Menorrhagia, Dysmenorrhea

Prospective, Non-interventional, Multi-center Safety Study of Mirena for Heavy Menstrual Bleeding and Dysmenorrhea

J-MIRAI
Start date: August 4, 2015
Phase:
Study type: Observational

The primary objective in this study is collecting post-marketing information on the safety. Thus, it includes information under the routine clinical practice on adverse events (AEs) and adverse drug reactions (ADRs) including expulsion and abnormal bleeding that occur within the first 12 months Mirena insertion. The secondary objective(s) in this study is/are collecting information on Mirena effectiveness, such as periodic blood loss and Quality of life (QOL), use of analgesic and dysmenorrhea pain as far as these are recorded under routine clinical practice.

NCT ID: NCT02473666 Completed - Hemorrhage Clinical Trials

Patient Blood Management - Use and Outcome

PBM-USZ
Start date: January 2012
Phase:
Study type: Observational

Study the influence of transfusion related Patient Blood Management Program actions on transfusion-related outcome measures and cost.

NCT ID: NCT02472184 Completed - Uterine Fibroids Clinical Trials

Optimal Order of Concurrent Office Hysteroscopy and Endometrial Biopsy

Start date: October 2015
Phase: N/A
Study type: Interventional

This study will look at the optimal order in which to perform concurrent office hysteroscopy and endometrial biopsy in female patients who present for evaluation of abnormal uterine bleeding at a fibroid and endometriosis treatment center.

NCT ID: NCT02468310 Completed - Pre-eclampsia Clinical Trials

Evaluating the Effects of SMS Text Messaging Support System Among Frontline Health Workers in Ghana

Accelerate
Start date: August 10, 2015
Phase: N/A
Study type: Interventional

Introduction Maternal and neonatal mortality continue to be to be prominent public health issues in sub Saharan Africa including Ghana, with slow progress made towards attainment of Millennium Development Goals (MDG) 4 & 5. Studies have identified poor quality of maternal and child healthcare as a major challenge to the prevention of neonatal and maternal deaths. Effective interventions are required to make significant inroads in these areas. Objective To evaluate the effect of a SMS text messaging intervention to support clinical decision making by frontline health care professionals on neonatal and maternal mortality. Methods We propose to conduct a randomized controlled trial in the Eastern region of Ghana, involving 8 intervention and 8 control districts. The intervention consists of text messaging of standard protocols for maternal and neonatal care to front line health care providers in the region. A total of 17,040 pregnant women who are receiving care (including antenatal, delivery and post-natal) at any of the hospitals in the selected districts in the region will be monitored through monthly aggregate data on outcome measures such as neonatal and maternal deaths from eclampsia, postpartum haemorrhage, puerperal sepsis, birth asphyxia, low birth weight and neonatal sepsis. Cord sepsis will also be included as neonatal sepsis for this study. Also, a quality of care assessment in four sampled districts to measure adherence to the safe motherhood protocol will be conducted. Stata software package.55 and MLwiN software version 2.2456 will be employed in data analysis. Descriptive analysis will be carried out to explore baseline characteristics of study groups while logistic regression will be applied to evaluate the effect of the intervention. A two-tailed statistical significant level of 0.05 will be used. Expected outcome We hypothesize that the intervention will improve both maternal and neonatal service delivery and health outcomes in the intervention areas.

NCT ID: NCT02465671 Completed - Cerebral Hemorrhage Clinical Trials

Prognostic Value of Plasma Thrombospondin-1 Levels After Acute Intracerebral Hemorrhage

Start date: August 2010
Phase: N/A
Study type: Observational

The current study was designed to investigate the change of plasma thrombospondin-1 levels and assess the prognostic predictive effect of plasma thrombospondin-1 levels in the patients with acute intracerebral hemorrhage.

NCT ID: NCT02461251 Completed - Hemorrhage Clinical Trials

Thromboelastometry-guided Treatment Protocol Versus Standard Care of Major Haemorrhage in Obstetric Patients

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

This is a prospective, randomized and controlled study to find out if a rotational thromboelastometry(ROTEM) guided treatment protocol reduces the need for blood transfusions in major obstetric haemorrhage compared to standard care of clinical decision making, conventional coagulation tests and massive transfusion protocol. Secondary aim is to find out if ROTEM can predict the incidence of thromboembolic events in this patient group.

NCT ID: NCT02456012 Completed - Clinical trials for Peptic Ulcer Hemorrhage

Long-term Oral Esomeprazole for Prevention of Peptic Ulcer Rebleeding in High-risk Patients

Eso_1y_R6PUB
Start date: April 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether a long-term prophylactic use of esomeprazole 20 mg twice daily or once daily has prevention effectiveness in reducing the recurrence of peptic ulcer bleeding after ulcer healed with 16-week oral esomeprazole therapy in high-risk patients whose Rockall score ≥ 6.