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NCT ID: NCT01311011 Recruiting - Clinical trials for Critical Limb Ischemia

Study of the Clinical Efficacy of Autologous SCT in Patients With Critical Limb Ischemia

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

Phase II Prospective Study of the Clinical Efficacy of Autologous SCT in patients with Critical Limb Ischemia

NCT ID: NCT01310985 Completed - Clinical trials for Colon Rectal Cancer Duke Stage Stageval

A Trial of Pre-Operative Chemoradiotherapy Using Capecitabine, Radiation & Cetuximab, in Rectal Cancer

Start date: March 2008
Phase:
Study type: Observational

A Pilot Trial of Pre-Operative Chemoradiotherapy Using Capecitabine (Xelodaâ), External Beam Radiation and Cetuximab (Erbitux®) Followed by Definitive Surgery in Patients With Localized (Non-Metastatic) Rectal Cancer

NCT ID: NCT01310972 Completed - Colon Cancer Clinical Trials

Adjuvant Colon Cancer w/ ELOXatin®/5 FU Based Regimen: ACCELOX

Start date: September 2007
Phase:
Study type: Observational

Adjuvant Colon Cancer With ELOXatin®/5 FU Based Regimen: ACCELOX

NCT ID: NCT01310959 Recruiting - Clinical trials for Aplastic Anemia and Other Marrow Failure Syndrome

Establishing a Data Base for Aplastic Anemia and Other Marrow Failure Syndrome

Start date: January 2003
Phase: N/A
Study type: Observational

Establishing a Data Base for Aplastic Anemia and Other Marrow Failure Syndrome

NCT ID: NCT01310946 Recruiting - Clinical trials for Acute Lymphocytic Leukemia

Establishment of Acute Lymphocytic Leukemia Data Base in the Department of Oncology

Start date: June 2003
Phase: N/A
Study type: Observational

Establishment of Acute Lymphocytic Leukemia Data Base in the Department of Oncology

NCT ID: NCT01285479 Recruiting - Multiple Sclerosis Clinical Trials

The Gilenya Pregnancy Registry

Start date: October 15, 2011
Phase:
Study type: Observational [Patient Registry]

The purpose of the Multi-National Gilenya Pregnancy Exposure Registry in Multiple Sclerosis (MS) is to continuously monitor, evaluate, and assess for major and minor teratogenic effects in the offspring of women exposed to fingolimod before (up to 8 weeks before last menstrual period (LMP)) and during pregnancy in routine clinical practice. The overall aim is to collect and evaluate data on maternal, fetal, and infant outcomes and compare it with reference populations.

NCT ID: NCT01275066 Completed - MPS IV A Clinical Trials

A Double-Blind Study to Evaluate the Efficacy and Safety of BMN 110 in Patients With Mucopolysaccharidosis IVA (Morquio A Syndrome)

Start date: February 2011
Phase: Phase 3
Study type: Interventional

This Phase 3 study will evaluate the efficacy and safety of 2.0 mg/kg/week BMN 110 and 2.0 mg/kg/every other week BMN 110 in patients with mucopolysaccharidosis IVA (Morquio A Syndrome). There is currently no standard accepted treatment for MPS IVA other than supportive care. Enzyme replacement therapy (ERT) may be a potential new treatment option for MPS IVA patients. BMN 110 is administered to MPS IVA patients by IV infusion, allowing cellular uptake by the mannose-6-phosphate receptor and transportation to the lysosomes. This enzyme uptake into the lysosomes is hypothesized to promote increased catabolism of keratan sulfate (KS) in tissue macrophages, hyaline cartilage, other connective tissues, and heart valve, and reduce the progressive accumulation of KS which is responsible for the clinical manifestations of the disorders.

NCT ID: NCT01272453 Completed - Clinical trials for Coronary Artery Disease

Computed Tomography Dose Reduction Using Sequential or Fast Pitch Sprial Technique

CTDOSE
Start date: January 2011
Phase: N/A
Study type: Observational

This is a prospective, controlled observational trial of patients undergoing clinically indicated cardiothoracic computed tomography (CT), including pulmonary or aortic angiography and coronary CT angiography (CCTA).

NCT ID: NCT01272037 Active, not recruiting - Clinical trials for Invasive Breast Carcinoma

Tamoxifen Citrate, Letrozole, Anastrozole, or Exemestane With or Without Chemotherapy in Treating Patients With Invasive RxPONDER Breast Cancer

Start date: January 15, 2011
Phase: Phase 3
Study type: Interventional

This randomized phase III clinical trial studies how well tamoxifen citrate, anastrozole, letrozole, or exemestane with or without chemotherapy work in treating patients with breast cancer that has spread from where it began in the breast to surrounding normal tissue (invasive). Estrogen can cause the growth of breast cancer cells. Hormone therapy, using tamoxifen citrate, may fight breast cancer by blocking the use of estrogen by the tumor cells. Aromatase inhibitors, such as anastrozole, letrozole, and exemestane, may fight breast cancer by lowering the amount of estrogen the body makes. Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. It is not yet known whether giving tamoxifen citrate, anastrozole, letrozole, or exemestane is more effective with combination chemotherapy in treating patients with breast cancer.

NCT ID: NCT01271621 Completed - Clinical trials for Effect of Intubation on Intraocular Pressure

Influence of Glidescope Assisted Endotracheal Intubation on Intraocular Presure

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

Tracheal intubation with traditional Macintosh laryngoscope is associated with increase in intraocular pressure along with tachycardia and hypertension. These effects are not desirable in ophthalmic patients especially in patients with glaucoma. GlideScope video laryngoscope system is a new approach for laryngoscopy and tracheal intubation. It does not require a direct line of sight to the glottis when intubating with the Glidescope and as a result intubation is much less stimulating to the patient. Therefore GlideScope video laryngoscope assisted intubation could be a preferable technique for intraocular surgery offering advantages in terms of intraocular pressure and cardiovascular stability.