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NCT ID: NCT01475799 Active, not recruiting - Clinical trials for Aortic Valve Stenosis

Percutaneous Aortic Valve 18F System for the Treatment of Patients With Severe Aortic Stenosis

Start date: November 2011
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the safety and performance of the Direct Flow Medical study valve and delivery procedure.

NCT ID: NCT01473797 Active, not recruiting - Clinical trials for Langerhans Cell Histiocytosis of Lung

Evaluation of Efficacy and Tolerance of Cladribine in Symptomatic Pulmonary Langerhans Cell Histiocytosis

ECLA
Start date: November 2011
Phase: Phase 2
Study type: Interventional

ECLA is a phase II, multicenter study testing sub cutaneous cladribine 0.1mg/kg/j during 5 days, administrated every month for 4 courses, in symptomatic adult patients with pulmonary Langerhans cell histiocytosis and impairment of lung function patients.

NCT ID: NCT01471860 Active, not recruiting - Heart Failure Clinical Trials

BAROSTIM NEO System in the Treatment of Heart Failure

Start date: August 2011
Phase: N/A
Study type: Interventional

The purpose of this portion of study NCT01471860 is to assess the long-term safety and efficacy of the BAROSTIM NEO System in Canadian study participants implanted with the device.

NCT ID: NCT01469936 Active, not recruiting - Fibromyalgia Clinical Trials

Effect of PERMEAPROTECT on the Quality of Life of Patients With Fibromyalgia

L2009-03
Start date: November 2011
Phase: N/A
Study type: Interventional

Fibromyalgia is a medical disorder characterized by chronic widespread pain, and a heightened and painful response to pressure. Fibromyalgia symptoms are not restricted to pain, leading to the use of the alternative term fibromyalgia syndrome for the condition. Other symptoms include functional gastrointestinal pain and discomfort. The origin of these symptoms is not yet known, and a few hypotheses have been stated. One of the supposed mechanisms that may lead to gastrointestinal hypersensitivity is a chronic, low-grade, intestinal inflammation due to an increased intestinal permeability. In this study, we hypothesise that the food supplement PERMEAPROTECT (that contains, amongst other nutrients, glutamine and curcumin) contributes to reducing the intestinal permeability and low-grade inflammation, thus improving gastrointestinal quality of life.

NCT ID: NCT01466179 Active, not recruiting - Clinical trials for Acute Lymphoblastic Leukemia

Clinical Study With Blinatumomab in Patients With Relapsed/Refractory B-precursor Acute Lymphoblastic Leukemia (ALL)

Start date: December 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to confirm whether the bispecific T cell engager antibody blinatumomab (MT103) is effective and safe in the treatment of patients with relapsed or refractory Acute Lymphoblastic Leukemia (ALL).

NCT ID: NCT01449344 Active, not recruiting - Clinical trials for Mantle Cell Lymphoma

Efficacy and Safety of R-HAD Alone or in Combination With Bortezomib in Patients With Relapsed or Refractory MCL

(R-HAD)
Start date: May 9, 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of rituximab, high-dose ara-c and dexamethasone (r-had) alone or in combination with bortezomib in patients with relapsed or refractory mantle cell lymphoma.

NCT ID: NCT01447940 Active, not recruiting - Clinical trials for Diabetes Mellitus, Type 1

Prospective Assessment of Meos Telemedicine E-portal on Ambulatory Care of Type 1 Diabetic Patients

TELEDIAB-3
Start date: January 2012
Phase: Phase 3
Study type: Interventional

Primary objective of TELEDIAB-3 study is to demonstrate that the use of Meos Telemedicine ePortal for sharing information between diabetologist and type 1 diabetic patient is not inferior to a conventional care regarding metabolic results at 12 months.

NCT ID: NCT01442246 Active, not recruiting - Metastases Clinical Trials

Evaluation of Adjuvant Hormonal Treatment for 24 Months After Radical Prostatectomy in High Risk of Recurrence Patients.

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

PRINCIPAL OBJECTIVE: Evaluation of effectiveness in terms of survival without metastases to 10 years, of adjuvant hormonal treatment with leuprorelin acetate (Eligard® 45 mg) for 24 months after radical prostatectomy in patients with high risk of recurrence. SECONDARY OBJECTIVE(S): - PSA evolution - Evaluation of testosterone level - Specific survival - Overall survival - Tolerance - Quality of life (QLQ-C30 questionnaires)

NCT ID: NCT01440413 Active, not recruiting - Breast Cancer Clinical Trials

Study of the Response to a Neoadjuvant Chemotherapy Based on the Antitumor Immune Response in Localized Breast Cancer

BREAST IMMUN
Start date: December 2011
Phase: N/A
Study type: Interventional

This is a prospective, non-randomized study which aims to evaluate the response to a neoadjuvant chemotherapy according to the the antitumor immune response in localized breast cancer. 40 patients will be enrolled in the study. They will receive chemotherapy : 3 or 4 anthracycline cycles or 3 or 4 FEC-100 cycles followed by 3 or 4 taxane cycles. Trastuzumab will be added to taxane for HER2+/Neu+ patients. Then, patients will be operated and receive an adjuvant treatment which will both depend on the investigator's appreciation. Blood sample will be collected on the first day of the first chemotherapy cycle, on the first day of the third cycle, on surgery, 6 months after the surgery and in case of relapse. Tumor sample will be collected on diagnosis as much as possible and on surgery. Patients will be followed during 5 years.

NCT ID: NCT01434420 Active, not recruiting - Breast Cancer Clinical Trials

Triple Negative Breast Cancer: Study of Molecular and Genetic Factors

Start date: March 2011
Phase: N/A
Study type: Interventional

Breast cancer triples negatives (TN; 15 % of the cases) are characterized by a high histoprognostic grade, a strong proliferation, a strong metastatic power, and a worse prognosis than the other forms of breast cancer. It is however a heterogenous group for histological and molecular level, but also for evolution. Most of the TN is part of the basal breast cancer subcategory. Until now, the medical treatment is based on chemotherapy. Breast cancers by constitutional mutation of BRCA1 / BRCA2 (5 % of breast cancers) are mostly of basal type and their prognostic seems better that what could be expected from high grade tumours and without hormonal receptors. They would be much more frequent in the TN group. However, at this day, no prospective study was led to estimate this incidence, or to study the intervention of other genes of predisposition, as well to analyse the links between this phenotype and their consequences at the germinal or somatic level, in terms of associated molecular changes and prognosis. The purpose of this study is, on a prospective study, to lead a joined analysis at the germinal level, in search of mutations of the main genes of breast cancer predisposition (BRCA1/2, PALB2, PTEN, PALB2), and at the tumour level (tissue micro-array and transcriptome), by correlating these results to the main clinical parameters. The 5 years relapse-free survival will also be estimated.