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NCT ID: NCT01295411 Active, not recruiting - Schizophrenia Clinical Trials

Morphological, Structural and Functional Neural Substrates of Quality of Life in Schizophrenia

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

The aim of the investigators analysis is to identify the neural correlates of quality of life scores in schizophrenia. For this, the investigators will constitute group of patients according to their quality of life scores and the investigators will analyze their differences in patterns of brain structures and activations.

NCT ID: NCT01295398 Active, not recruiting - Clinical trials for Acute Viral Bronchiolitis

Influence of the Nebulizer on the Clinical Efficacy of Hypertonic Saline 3% in Children Aged Less Than 18 Months and Hospitalized With Acute Viral Bronchiolitis

Start date: December 2010
Phase: N/A
Study type: Interventional

The aim of the investigators study is to compare in children aged less than 18 months and hospitalized for an acute viral bronchiolitis the efficacy of the HS 3% (Mucoclear®, sterile ampoules of 4 ml) nebulised with a conventional jet-nebulizer (particles diameter of 4-5 µm), or with a jet-nebulizer adapted for infants (particles diameter of 2-2.5 µm), or with a mesh-nebulizer adapted for infants (particles diameter of 2-2.5 µm).

NCT ID: NCT01294748 Active, not recruiting - Clinical trials for Coronary Artery Disease

Clinical Investigation of the MiStent Drug Eluting Stent (DES) in Coronary Artery Disease

DESSOLVE-II
Start date: February 2011
Phase: Phase 2
Study type: Interventional

The DESSOLVE II clinical trial is to assess the safety and performance of the sirolimus-eluting MiStent for the treatment for improving coronary luminal diameter in patients with symptomatic ischemic heart disease due to discrete de novo lesions in the native coronary arteries.

NCT ID: NCT01294020 Active, not recruiting - Clinical trials for Kidney Transplantation

Study to Compare the Pharmacokinetics of Tacrolimus in Stable Pediatric Allograft Recipients Converted From Prograf® to Advagraf®

Start date: May 25, 2011
Phase: Phase 2
Study type: Interventional

Parts A & B: Conversion of stable pediatric allograft recipients from Prograf® immunosuppression to Advagraf® immunosuppression to compare exposure and one year follow-up for safety and efficacy. Part C: Continuation of long-term follow-up and provision of ongoing study medication to subjects to whom Advagraf® is currently not available.

NCT ID: NCT01291576 Active, not recruiting - Clinical trials for Endometriosis, Rectum

Functional Outcomes of Surgical Management of Deep Endometriosis Infiltrating the Rectum

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

The purpose of this study is to determine whether performing colorectal resection in deep endometriosis infiltrating the rectum is responsible for a higher rate of postoperative digestive and urinary dysfunction when compared to rectal nodules excision (conservation of the rectum).

NCT ID: NCT01291459 Active, not recruiting - HIV Clinical Trials

Pilot Study of Maraviroc/Raltegravir for Naive HIV-1 Patients

NNNB
Start date: September 2011
Phase: Phase 2
Study type: Interventional

Background and Rationale Raltegravir and Maraviroc, the first in class of 2 new families of antiretroviral drugs have demonstrated a high potency in treatment experienced and naive patients. Both drugs appeared well tolerated with low metabolic toxicity. No data are currently available concerning the combination of these 2 drugs. Hypothesis Maraviroc + Raltegravir should be potent enough to maintain virological efficacy in naive patients infected by CCR5 HIV-1 previously treated for 6 months with a Maraviroc-Raltegravir-Tenofovir-Emtricitabine combination.

NCT ID: NCT01289522 Active, not recruiting - Clinical trials for Squamous Cell Head and Neck Carcinoma

Chemotherapy With Cetuximab in Treating Patients With Recurrent or Metastatic Head and Neck Cancer

Start date: September 2009
Phase: Phase 2
Study type: Interventional

PURPOSE: Cetuximab with platinum and 5FU is now the standard combination as first-line treatment in patients with metastatic or recurrent Head and Neck squamous cell carcinomas. Cetuximab and taxane combinations have demonstrated promising activity in Head and Neck cancer. This phase II trial is studying new cetuximab, docetaxel and cisplatin combination named TPEx as first-line treatment in this setting.

NCT ID: NCT01286753 Active, not recruiting - Neoplasms Clinical Trials

A Study of RO5185426 (Vemurafenib) in Patients With Metastatic or Unresectable Papillary Thyroid Cancer Positive for the BRAF V600 Mutation

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

This open-label, multi-center study will evaluate the safety and efficacy of RO5 185426 in patients with metastatic or unresectable papillary thyroid cancer posi tive for the BRAF V600 mutation and resistant to radioactive iodine therapy. Pat ients will receive RO5185426 960 mg orally twice daily until progressive disease or unacceptable toxicity occurs.

NCT ID: NCT01284725 Active, not recruiting - Nephritis of Lupus Clinical Trials

Weaning of Immunosuppression in Nephritis of Lupus

WIN-Lupus
Start date: January 2011
Phase: Phase 3
Study type: Interventional

The investigators wish to evaluate the discontinuation of maintenance immunosuppressive treatment after 2 years in patients with stable remission after a proliferative lupus nephritis. The patients will be continuing their treatment with hydroxychloroquine, possibly associated with low dose corticosteroids.

NCT ID: NCT01284712 Active, not recruiting - Polycythemia Vera Clinical Trials

Natural Killer Cells and Polycythemia Vera (Vaquez's Disease)

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

Natural Killer cells (NK) are pivotal cells of innate immunity, that sense defective expression of HLA class I molecules and are complementary to specific cytotoxic T lymphocytes. A defect in NK cell cytotoxicity has been described in some hematopoietic malignancies such as acute myeloid leukemia, multiple myeloma, myelodysplastic syndroms. This defect is at least partially linked to a decreased or absent expression of some activating NK cell molecules, more particularly the so-called Natural Cytotoxicity Receptors (NCRs) NKp30, NKp44 and NKp46. Some old publications have demonstrated defective NK cytotoxicity in myeloproliferative syndroms (chronic myeloid leukemia, primary thrombocytosis, polycythemia vera). The investigators more particularly focused their attention on polycythemia vera (Vaquez's disease), a myeloproliferative disease characterized by the recently describet mutation V617F of the JAK2 tyrosine kinase. The investigators will precise the mechanisms leading to this cytotoxicity defect, the investigators also will evaluate the implication of V617F mutation on NK physiology, and will study the interactions between NK cells and hematopoietic progenitors.