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Hematologic Diseases clinical trials

View clinical trials related to Hematologic Diseases.

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NCT ID: NCT01314534 Completed - Kabuki Syndrome Clinical Trials

French Kabuki Syndrome Network. Epidemiology, Management of Patients and Research by Array-CGH

Kabuki
Start date: September 2008
Phase: N/A
Study type: Observational

Create a census for the duration of the search for French patients with SK - determining epidemiological and morphological parameters, - determine the true frequency of clinical symptoms and identify new ones, - identify complications of the disease to improve the care of patients in the hope of a better prognosis of the disease and - performing a radiological study by Voxel based morphometry MRI type (N. BODDAERT, HOPITAL Necker-Enfants Malades, Paris) Perform genetic research to identify the genetic bases of SK using CGH-array (Comparative Genomic Hybridization )

NCT ID: NCT01254318 Completed - Leukemia Clinical Trials

Assessment of the Fungal Infection Incidence Across Canada for High Risk Subjects With Hematological Disease (Study P07501)

TRAFIC
Start date: March 2013
Phase: N/A
Study type: Observational

This will be a retrospective study that includes retrospective chart reviews at major institutions across Canada. The intent of the study is to generate both regional and national incidence data for non-Candida invasive fungal infections (IFI) in high risk subjects. The study will include participants receiving stem cell transplant and high dose chemotherapy treatment for leukemia.

NCT ID: NCT01224496 Completed - Clinical trials for Myelodysplastic Syndrome (MDS)

Traditional Chinese Medicine in the Supportive Management of Anaemic and Cytopenic (Leukopenia, Thrombocytopenia) Haematological Disorders

Start date: July 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to study the efficacy of Traditional Chinese Medicine (TCM) on anaemic and cytopenic haematological disorders including myelodysplastic syndrome (MDS), aplastic anaemia (AA), myelofibrosis (MF) and thalassemia intermedia who do not have or did not respond to available treatment options.

NCT ID: NCT01220011 Completed - Clinical trials for Infant, Newborn, Diseases

Randomized Controlled Trial Comparing a Conservative Management and Laser Surgery

TTTS1
Start date: April 19, 2011
Phase: N/A
Study type: Interventional

The objective of this trial is to compare both strategies (Expectative Vs Fetoscopic laser surgery) for patients with stage 1 TTTS and favorable obstetrical parameters in an international randomized controlled trial. This trial will answer an important question and will help in the management and tailoring of surgical indications in stage 1 TTTS.

NCT ID: NCT01210716 Completed - Autoimmune Diseases Clinical Trials

Evaluation of Therapeutic Plasma Exchange (TPE) Procedure Using the AMICUS Device

Start date: September 2010
Phase: Phase 3
Study type: Interventional

This study will evaluate the use of the AMICUS device in patients where Therapeutic Plasma Exchange (TPE) is prescribed by their physicians.

NCT ID: NCT01178177 Completed - Hematologic Disease Clinical Trials

Radiologic Features of Invasive Pulmonary Aspergillosis

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

Invasive pulmonary aspergillosis (IPA) is an opportunistic infection that primarily affects recipients of solid organ transplants (SOTs) and patients with chemotherapy- induced neutropenia.Although both of these populations are at high risk for IPA, they differ with regards to the specific defects in host defense mechanisms that increase their risk for IPA. Chemotherapy- induced neutropenia is the principal defect affecting patients with hematologic malignancies, whereas transplant recipients tend to have dysfunctional T cells and phagocytes, as a result of immunosuppressive drug therapy. Thus, the patterns of IPA-related infection and inflammation may differ according to the type of underlying immune defect. Although the clinical and radiological features of IPA in patients with neutropenia have been extensively studied, little is known about the characteristics of IPA in SOT recipients. The investigators therefore compared the IPA- related clinical and radiological findings in SOT recipients with those of neutropenic patients.

NCT ID: NCT01167218 Completed - Clinical trials for Platelet Aggregation Defects

Study to Assess Platelet Dysfunction With Verify Now Assay

Start date: December 2009
Phase:
Study type: Observational

The purpose of this study is to conduct a Verify now assay to detect platelet aggregation defects in patients with Myelodysplastic syndrome(MDS), immune thrombocytopenia purpura (ITP) and myeloproliferative disorders (MPD).

NCT ID: NCT01114165 Completed - Sepsis Clinical Trials

Value of the LightCycler® SeptiFast Test MGRADE for the Pathogen Detection in Neutropenic Hematological Patients

Start date: May 2010
Phase: Phase 4
Study type: Interventional

The overall objective of this study is to assess the clinical value of the SeptiFast Test as an adjunct to traditional microbiological, clinical, and other laboratory assessments in early detection and identification of a potential pathogen and therefore early targeted antimicrobial management of neutropenic hematological patients with suspected infection or sepsis.

NCT ID: NCT01108159 Completed - Clinical trials for Hematologic Diseases

Integrated Whole-Genome Analysis of Hematologic Disorders

Start date: September 2009
Phase:
Study type: Observational

We will use new technologies to look at the DNA, RNA, proteins, and metabolites in the disease-containing blood, bone marrow, or tissue and normal cells from the skin. Our goal is to analyze all of the genes in the diseased and normal skin sample. By comparing the results of the diseased sample and normal skin cells and the results of the two types of genetic information (DNA and RNA), we should be able to identify genetic changes that are important for the initiation, progression, or treatment response of that particular disorder.

NCT ID: NCT00994136 Completed - Hematologic Disease Clinical Trials

Safety of Catheter Lock With or Without Heparin in Implanted Central Venous Catheters

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

Long-term central venous access devices are considered as safe for the administration of medication as chemotherapy, but are also used for blood sampling. For years these catheters have been locked with a heparin solution in order to avoid occlusion. However, no scientific evidence supports heparin locking when the device is not in use. Advanced technology as needleless caps and valved catheters and port reservoirs confirms this trend to use 'saline only' for locking these devices. Therefore the investigators hypothesize is that there will be no difference in proportion of occlusions and catheter related bacteremia in long-term venous access devices locked with 'saline only' versus with heparin.