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Hemorrhage clinical trials

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NCT ID: NCT04748081 Completed - Clinical trials for Surgery--Complications

The Major Bleeding Risk Following Hepatectomy

Start date: January 1, 2000
Phase:
Study type: Observational

This study examined long-term incidence rates of major bleeding associated with hepatectomy. The investigators used data from Taiwan's National Health Insurance Research Database. Patients who underwent hepatectomy between 2000 and 2012 were identified by International Classification of Diseases, Ninth Revision, Clinical Modification codes. Variables including gender, age, comorbidities, and prescribed medications were matched between cases and controls. A total of 1,053 patients with hepatectomy and 4,212 matched non-hepatectomy subjects were included in this study.

NCT ID: NCT04741334 Completed - Cerebral Hemorrhage Clinical Trials

Mild Head Injury, Antiplatelets, and Anticoagulants

Start date: September 27, 2019
Phase:
Study type: Observational

Approximately 20% of patients with mild head injury presenting to the Emergency Department (ED) is taking antiplatelet agents and 10% is taking oral anticoagulants. The aim of the study is to determine the prevalence of cerebral hemorrhage in patients presenting to the ED with an MHI. It also aims to determine whether the use of antiplatelet agents and anticoagulants may be a risk factor for the occurrence of cerebral hemorrhage and mortality. This is a prospective observational study that will include all patients who present to ED at Gemelli Hospital for an MHI for 2 years. Patients will be divided into four groups according to whether or not they are taking anticoagulants and antiplatelet drugs. Groups will be compared to evaluate the possible increased risk of complications in patients on treatment and among the different medications.

NCT ID: NCT04734535 Completed - Surgical Bleeding Clinical Trials

Evaluation of Safety of HEMOBLAST Bellows in Spine Surgery

Start date: March 8, 2021
Phase: N/A
Study type: Interventional

The purpose of this clinical investigation in open, elective, spine surgery is to collect data to support the removal of the neurosurgical exclusion from the currently approved indication for the use of HEMOBLASTâ„¢ Bellows. This study is primarily designed to assess safety of the device for use in spine surgery, although efficacy information will also be captured and reported.

NCT ID: NCT04733157 Completed - Clinical trials for Postpartum Hemorrhage

The Efficacy of Tranexamic Acid in Preventing Postpartum Haemorrhage After Caesarean Section

ETAPPH
Start date: March 23, 2021
Phase: Phase 3
Study type: Interventional

This study seeks to determine if the using tranexamic acid prophylactically at caesarean section will prevent postpartum haemorrhage which is a major cause of maternal mortality in Zimbabwe and globally.

NCT ID: NCT04725929 Completed - Placenta Previa Clinical Trials

Vaginal Progesterone Against a Second Attack of Antepartum Haemorrhage in Placenta Previa Women

Start date: January 1, 2021
Phase:
Study type: Observational [Patient Registry]

Placenta praevia is associated with an increased risk of preterm delivery (PTD) especially if associated with bleeding and uterine contractions . In this study we will determine the effect of Progesterone in preventing a second attack of antepartum haemorrhage in pregnant women diagnosed with placenta previa

NCT ID: NCT04723979 Completed - Clinical trials for Post Partum Hemorrhage

NovoSeven® in Severe Postpartum Haemorrhage - Experiences From UK, DK, FR, NL

Start date: May 1, 2020
Phase:
Study type: Observational

The overall aim of this project is to include currently available information from women with severe postpartum haemorrhage (sPPH) who were treated with NovoSeven® and to examine whether NovoSeven® may have affected the course of the PPH in these women, specifically the control of bleeding. Data will be included from previous cohort studies from four countries: United Kingdom (UK), the Netherlands, Denmark, and France.

NCT ID: NCT04720885 Completed - Pregnancy Related Clinical Trials

Management of Large Retained Products of Conception (> 4 cm): Need for an Standardized Procedure.

Start date: December 28, 2020
Phase:
Study type: Observational

Collection of relevant data form patients who were treated in the Ghent University Hospital in the context of a placental remnant lager than 4 cm, performing statistical analyzes on the collected data, reviewing the literature on the subject and formulation of a recommendation for treatment of these large placental remnants.

NCT ID: NCT04712786 Completed - Refractive Errors Clinical Trials

Refractive Changes Following Vitrectomy

Start date: December 1, 2020
Phase:
Study type: Observational

We aimed o compare the refractive changes associated with pars plana vitrectomy with or without intraocular gas tamponade in pseudophakic eyes. This retrospective study included pseudophakic patients with Nd:YAG laser posterior capsulotomy who underwent 23G PPV between February 2015 and March 2019. Group 1 consisted of patients with regmatogenous RD who underwent PPV and 12% perflouropropane (C3F8) gas tamponade whereas Group 2 consisted of patients who underwent PPV for epiretinal membrane or vitreous hemorrhage (VH). No tamponade was used in Group 2. Minimum follow-up was 12 months.

NCT ID: NCT04710017 Completed - Uterine Bleeding Clinical Trials

Tranexamic Acid and Depot-Medroxyprogesterone Acetate for Perimenopausal Irregular Uterine Bleeding

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

Abnormal uterine bleeding is a symptom and not a disease. It is one of the most frequently encountered complaints in gynecologic practice. It accounts for more than 70% of all gynecological consultations in the peri- and post-menopausal age group. Abnormal uterine bleeding may be acute or chronic and is defined as bleeding from the uterine corpus that is abnormal in regularity, volume, frequency, or duration and occurs in the absence of pregnancy. Chronic heavy or prolonged uterine bleeding can result in anemia, interfere with daily activities. Iron deficiency anemia develops in 21 to 67 percent of cases and raises concerns about uterine cancer. According to the International Federation of Obstetrics and Gynecology, the classification of abnormal uterine bleeding is based on PALM-COEIN which is an acronym for various etiologies namely polyp, adenomyosis, leiomyoma, malignancy and hyperplasia, coagulopathy, ovulatory dysfunction, endometrial disorders, iatrogenic and not otherwise classified (PALM-COEIN).

NCT ID: NCT04706221 Completed - Blood Loss Clinical Trials

Clinical Evaluation of the CM-1500 in Postoperative Surgery Patients

Start date: January 15, 2021
Phase: N/A
Study type: Interventional

The primary objective is to evaluate the the changes in the Relative Index in post abdominal or pelvic surgery patients on the Cardiac Monitor Model CM-1500.