Clinical Trials Logo

Hematological Diseases clinical trials

View clinical trials related to Hematological Diseases.

Filter by:

NCT ID: NCT00956358 Completed - Clinical trials for Hematological Diseases

Study on Systemic and Airway Biomarkers in Haemopoietic Stem Cell Transplantation

Start date: March 2009
Phase: N/A
Study type: Observational

Haemopoietic stem cell transplantation (HSCT) has become a major life-saving treatment for many haematological conditions, mostly malignancies. However, there are lots of potential complications that hinder the long-term success of HSCT, in which bronchiolitis obliterans syndrome (BOS) is one of such serious complications. Basically, BOS represents a form of graft-versus-host immunological damage of small airways (bronchioles), leading to progressive narrowing of small airways and thus obstructive lung function abnormalities. With progressive loss of lung function in BOS, patients after HSCT can be complicated by intractable respiratory failure that results in mortality. Up until now, there is still no reliable way to accurately predict or detect BOS early to allow pharmacological interventions. Therefore there is intense interest in the search for biomarkers that can help to predict the occurrence of BOS after HSCT. Apart from biomarkers (e.g., cytokines) in blood, there has been recent development in the sampling of airway lining fluid by a non-invasive method, i.e., collection of exhaled breath condensate (EBC). In airway diseases such as asthma or chronic obstructive pulmonary disease, EBC has been found to have various cytokines which can serve as potential biomarkers of disease activity. Since BOS is largely a small airway disease, it becomes logical to investigate the profile of biomarkers in EBC as predictors for BOS after HSCT. Therefore this study has been designed to look into the role of biomarkers in blood and EBC in early detection of BOS after HSCT.

NCT ID: NCT00892502 Completed - Multiple Myeloma Clinical Trials

Can Treatment With Bismuth Reduce Toxicity to Chemotherapy and Radiotherapy?

Bismuth-PBH
Start date: May 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether treatment with Bismuth can reduce the toxicity of chemotherapy and radiotherapy in patients with malignant diseases of the blood.

NCT ID: NCT00884364 Recruiting - Clinical trials for Hematological Malignancies

Exercise During Chemotherapy for Patients With Hematological Malignancies

Start date: May 2009
Phase: Phase 3
Study type: Interventional

The trial will evaluate the effects of aerobic exercise in patients undergoing chemotherapy for the treatment of a hematological neoplastic disease.

NCT ID: NCT00838643 Active, not recruiting - Clinical trials for Invasive Aspergillosis

Invasive Aspergillosis After Allogeneic Hematopoietic Stem Cell Transplantation (HSCT)

Start date: May 2002
Phase: N/A
Study type: Observational

Evaluation of incidence of invasive aspergillosis in patients who have undergone an allogeneic stem cell transplantation, with particular regard to the role of galactomannan assay and of early TC scan in asymptomatic patients.

NCT ID: NCT00675038 Completed - Clinical trials for Hematological Diseases

Pilot Study of Non-Invasive Assessment of Hepatic And Myocardial Iron Through T2* Magnet Resonance Imaging (MRI) In Patients With Iron Overload

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

Many hematological disorders are treated by giving red blood cells. Over a long period of time iron from the red blood cell will accumulate in the tissues of the heart, liver, and endocrine glands. This condition is referred to as iron overload and may become life threatening due to the effects of the iron on these tissues. The normal method for evaluation of iron overload is a liver biopsy. This procedure is invasive and has potential risks, such as bleeding and infection. It is very desirable to establish a method for assessing iron overload which is not invasive. New magnet resonance imaging (MRI) relaxation techniques (T2*MRI) can be used to indirectly assess the liver iron content and iron in the heart. Results of T2*MRIs show excellent correlation with liver iron content and heart function. The use of this method of assessment will minimize the risk and inconvenience of liver biopsy and possibly allow more frequent evaluations for iron overload, thus better treatment for these patients. Participants in this study will undergo both liver biopsy for liver iron content and T2* MRI of the liver and the heart. Results from the procedures performed in this study will be compared, with the end result being the possible elimination of invasive procedures to diagnose iron overload.

NCT ID: NCT00390988 Completed - Healthy Volunteers Clinical Trials

Capillary and Venous Blood Count Parameters

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

The purpose of this study is to compare capillary blood count parameters with the corresponding venous samples to verify the hypothesis that capillary and venous blood count parameters are equivalent.