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Thrombophilia clinical trials

View clinical trials related to Thrombophilia.

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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.

NCT ID: NCT00683397 Completed - Clinical trials for Venous Thromboembolism

Frankfurt Thrombophilia Registry

Start date: May 2008
Phase: N/A
Study type: Observational

Consecutive patients with acute or previous venous thromboembolism are enrolled in this registry. Using a standardized questionnaire, clinical data detailing venous thromboembolism and contributing VTE risk factors are recorded. Results of technical and laboratory investigations including screening for thrombophilic disorders were additionally entered into the database.

NCT ID: NCT00485446 Completed - Clinical trials for Thrombophilia, Thyroid Autoimmunity

Thrombophilia and Thyroid Autoimmunity in Implantation Failure and Recurrent Miscarriage

Start date: n/a
Phase: N/A
Study type: Observational

This study was designed to evaluate the incidence of both, inherited and adquired thrombophilia, and thyroid autoinmunity in unknown infertility (UI), implantation failure (IF) and recurrent miscarriage (RM). To focus on these particular disorders and to rule out another potential confounding variables, 4 particular groups of women were created. Only young women (< 38 years old), patients whose previous preimplantation genetic screening (PGS) cycles displayed an acceptable rate of aneploidies, and women without organic uterine abnormality, autoimmune disease or endocrine disorder were included in the study.

NCT ID: NCT00457184 Completed - Migraine Clinical Trials

Thrombophilia and Migraine, Are They Related?

Start date: January 2004
Phase: N/A
Study type: Observational

Migraine was described as related to stroke in adults and children as well. Complete thrombophilic status was not study in large groups of pediatric patients. The purpose of our study is to assess the prethrombotic profile among children and teenagers diagnosed as suffering from migraine attacks.

NCT ID: NCT00400504 Recruiting - Cancer Clinical Trials

Hypercoagulability and Thromboembolic Risk in Patients With Malignant Disease, Evaluated by Thrombelastograph (TEG®)

Start date: November 2006
Phase: N/A
Study type: Observational

Patients with malignancies are at high risk of developing a thromboembolic complication and their treatment with chemo- and or radiation therapy further enhances this risk. Conventional haemostatic tests are not suitable as a screening tool of a hypercoagulable state. A hypercoagulable profile identified with the whole blood Thrombelastograph (TEG) Analyzer parameter maximal amplitude (MA) is reported to correlate with thrombotic events in patients undergoing major non-cardial surgery and recurrent ischemic events in patients undergoing percutaneous coronary intervention. In this study we investigate the correlation between TEG measurements and thromboembolic events in patients with newly diagnosed malignancies. The hypotheses of this study are: 1. Patients with malignancies and hypercoagulability, defined as a TEG MA>69 mm and /or R<4 min is at increased risk of developing thromboembolic complications as compared to those with a MA<69 mm and/or a R>4 min. 2. Hypercoagulability and hence TEG R and MA values are affected by the treatment instituted in these patients (chemo and radiation therapy) rendering the patients more hypercoagulable and hence at increased risk of developing thrombotic complications.

NCT ID: NCT00356434 Terminated - Thrombophilia Clinical Trials

A Comparison of Sequential Compression Devices and Foot Pumps in the Obstetric Population

Start date: November 2008
Phase: N/A
Study type: Interventional

The researchers at Johns Hopkins University believe that the foot pump will be superior to sequential compression devices in comfort and patient compliance which may increase provider efforts to prevent deep vein thrombosis (DVT) in pregnancy.

NCT ID: NCT00354796 Recruiting - Atrial Fibrillation Clinical Trials

The Effect of Reduced Dose of Enoxaparin on the Outcomes of Treatment With Enoxaparin

Start date: July 2006
Phase: N/A
Study type: Observational

We hypothesize that reduced dose of enoxaparin in elderly patients will result in reduced proportion of patients with therapeutic anti Xa activity and reduced clinical efficacy.

NCT ID: NCT00210197 Completed - Breast Cancer Clinical Trials

Hypercoagulability After Breast Cancer Surgery

EHC
Start date: January 2005
Phase: N/A
Study type: Observational

The risk of deep venous thrombosis after radical breast surgery is known. The objective of this study is to explore hypercoagulability after radical breast cancer surgery by studying several factors for haemostasis before, during and after surgery. Ultrasound Doppler examination is realised between 24 and 72 hours post-operatively. Hypercoagulability is defined by a significant increasing level of thrombin-antithrombin, D-dimer and the endogen thrombin potential.