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Thrombophilia clinical trials

View clinical trials related to Thrombophilia.

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NCT ID: NCT01799655 Completed - Chest Pain Clinical Trials

Does Vitamin D Deficiency Associated With Hypercoagulability & Increased Thrombin Generation?

Start date: April 2013
Phase: N/A
Study type: Observational [Patient Registry]

Cardiovascular disease is the most common cause of mortality and morbidity worldwide. Recently, a growing body of evidence has identified Vitamin D deficiency as a potential risk factor for cardiovascular disease. Therefore, there is an increasing interest to explore the mechanism in which vitamin D deficiency affect the cardiovascular system. The investigators want to examine the relationship between serum vitamin D levels and the coagulation status in the subjects. The applied the calibrated automated thrombogram (CAT) to assess thrombin generation in plasma as a measure of overall thrombotic activity, and thus to suggest a mechanism that may explain the link between vitamin D deficiency and cardiovascular disease. Our study population are going to include 100 patients from the internal departments in Emek hospital, who present with chest pain but without acute coronary syndrome (ACS). The investigators will take blood samples from the subjects to measure the serum vitamin D levels and the generation of thrombin. The patients will be divided into four groups according to the level of vitamin D to evaluate the effect of vitamin D levels in the blood on coagulability and thrombotic activity in these patients.

NCT ID: NCT01722669 Completed - Healthy Clinical Trials

Quercetin PK/PD Study in Healthy Adults and Patients With Hypercoagulable States

PK/PD
Start date: May 2012
Phase: Early Phase 1
Study type: Interventional

The goal of this study is to evaluate how much quercetin or isoquercetin is absorbed after a single dose and evaluate for pharmacokinetic inhibition of protein disulfide isomerase. Pharmacodynamic studies will also be performed in an additional cohort of 10 patients with evidence of antiphospholipid antibodies

NCT ID: NCT01487291 Completed - Insulin Resistance Clinical Trials

Prevalence of Clinical and Laboratory Markers of Hypofibrinolysis in Psychotic Patients

Start date: January 2013
Phase: N/A
Study type: Observational

At the Thrombophilia Clinic of the Hospital Federal dos Servidores do Estado do Rio de Janeiro there is a high prevalence of acute psychotic episodes, which allows the investigators to raise the suspicion that the thrombotic tendency or hypofibrinolysis play a role in the onset of the disease. It is striking that most of these patients, after some time on anticoagulants, no longer need to take psychiatric medication.

NCT ID: NCT01475149 Completed - Clinical trials for Systemic Lupus Erythematosus

Effect of HCQ on AnxA5 Resistance Assay in Antiphospholipid (aPL) Positive Patients With and Without Systemic Lupus Erythematosus (SLE)

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

This 12 week study will observe patients with and without systemic lupus erythematosus who have persistent antiphospholipid antibodies in the blood who are starting a medicine called hydroxychloroquine. It will measure if these patients have a change in a blood test called the annexin A5 resistance assay over that 12 week period.

NCT ID: NCT01416454 Completed - Thrombophilia Clinical Trials

Thromboelastography to Assess Age-Related Coagulation Differences in Patients Undergoing Cesarean Delivery

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

The purpose of the study is to assess potential age-related differences on coagulation profile of patients undergoing Cesarean Section, using thromboelastography (TEG). The investigators will compare coagulation data collected from the study to assess potential differences in coagulation parameters for the following age groups: (i) women less than 35 yrs (ii) women 35 yrs or older.

NCT ID: NCT01372553 Completed - Breast Cancer Clinical Trials

Guilford Genomic Medicine Initiative (GGMI)

GGMI
Start date: October 2009
Phase: Phase 4
Study type: Observational

- Genomic medicine, using genetic information to improve health outcomes, is heralded as the answer to rising medical costs by focusing on prevention and tailored care. Despite its potential, little investigation has focused on how genomic medicine can be applied in health care. To be effective, it requires new ways to learn, deliver, and communicate medical information. It will also raise new ethical questions. - The overall goal of Guilford Genomic Medicine Initiative (GGMI) is to identify the specific challenges in "re-structuring" an existing medical system to integrate genomic medicine, and create solutions that can be used by other medical systems, such as the extensive military medical care system. To accomplish this goal, GGMI includes the development of a large-scale genomic medicine education initiative targeted at the community, providers, and patients, and a clinical systems model to implement strategies to facilitate the integration of genomic medicine into several pilot practices.

NCT ID: NCT01214772 Completed - Pregnancy Clinical Trials

The Effect of Heparin in Treatment IVF-ET Failure

Start date: May 2009
Phase: Phase 4
Study type: Interventional

Embryo transfer failure is defined as ≥3 IVF-embryo transfer failures without pregnancy . In spite of transfer of 3 good quality embryos , just 20-30% of women undergoing IVF will achieve ongoing pregnancy . There are multiple factors that influence IVF-failure. Autoantibodies may be one of the possible causes of IVF-failure , especially in unexplained and mechanical infertility . In some studies , antiphospholipid antibody is considered as causative factor on implantation and embryo failure. However some investigators showed that combination therapy with heparin/aspirin in women with positive antiphospholipid antibody is not effective in improving of IVF-outcome . In prospective studies were not confirmed association between antiphospholipid antibody abnormalities and IVF-failure. Recently has been relationship between thrombophilia and IVF and implantation failure. The effect of unfractionated heparin in assisted reproductive technology (ART) cycles is prevention of thrombosis in implantation site . Although its effect is not restricted to anticoagulation and also can modulate apposition , adhesion , and penetration of embryo . Other advantages are decreasing thrombophilic risk in COH ( controlled ovarian hyperstimulation) cycles with administration of gonadotrophins . So heparin make better pregnancy rate in repeated IVF-ET failures. There are few studies in regard to heparin effects on IVF cycles outcome . The purpose of this study is evaluation of unfractionated heparin effects on improvement of ART outcome . This study was a prospective randomized controlled trial to assess whether administration of heparin would increased pregnancy rates in women with repeated ET-IVF failures.

NCT ID: NCT00967382 Completed - Pregnancy Clinical Trials

TIPPS: Thrombophilia in Pregnancy Prophylaxis Study

TIPPS
Start date: July 2000
Phase: Phase 3
Study type: Interventional

The TIPPS trial seeks to determine the safety and effectiveness of low-molecular-weight heparin (LMWH), an anticoagulant, in preventing placenta mediated pregnancy complications and venous thromboembolism (VTE) in women with thrombophilia. Thus, the principal research question is: can LMWH prevent thrombosis in the leg veins, pulmonary arteries and placental vessels, thereby reducing the risk of deep vein thrombosis, pulmonary embolism (PE), intrauterine growth restriction (IUGR), preeclampsia, miscarriage and stillbirth?

NCT ID: NCT00883272 Completed - Menopause Clinical Trials

Effect of DT56a (Femarelle) on the Coagulation System in the Treatment of Postmenopausal Women

Start date: January 2007
Phase:
Study type: Observational

The purpose of this study is to determine if Femeralle (DT56a) has an effect on the coagulation system, measured by platelet adhesion and aggregation, of normal and thrombophilic postmenopausal women.

NCT ID: NCT00721591 Completed - Clinical trials for Recurrent Pregnancy Loss

Pharmacokinetics of Low Molecular Weight and Unfractionated Heparin in Pregnancy

Start date: March 2005
Phase: N/A
Study type: Observational

To determine, through pharmacokinetic parameters, the ideal dosing protocol for dalteparin (a low molecular weight heparin) and unfractionated heparin for women desiring pregnancy who have evidence of an acquired (specifically, antiphospholipid syndrome) or inherited thrombophilia.