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NCT ID: NCT00665041 Completed - Clinical trials for Ovarian Hyperstimulation Syndrome

Tolerability of Quinagolide in a Dose-titration Regimen in Oocyte Donors at Risk of Developing Ovarian Hyperstimulation Syndrome

Start date: May 2008
Phase: Phase 2
Study type: Interventional

Assess the tolerability of quinagolide 200 μg/day in a dose-titration regimen in oocyte donors undergoing controlled ovarian hyperstimulation and at risk of developing OHSS Secondary Objectives Estimate the effects of a quinagolide dose-titration regimen compared to placebo in peritoneal fluid accumulation, incidence of ascites, OHSS symptoms and clinical laboratory parameters of haemoconcentration

NCT ID: NCT00664534 Completed - Clinical trials for Diabetes Mellitus, Type 2

Pre-Mix Insulin Lispro Treatment for Type 2 Diabetes Patients Who Consume a Light Breakfast

Start date: April 2008
Phase: Phase 4
Study type: Interventional

This study is designed to look at how best to start and then gradually intensify (as needed) the insulin lispro premix regimen in type 2 diabetes patients who consume a light breakfast.

NCT ID: NCT00663559 Completed - Clinical trials for Carcinoma Renal Cells

Sunitinib in Patients With Renal Cells Carcinoma Metastasic or Locally Avanced in Patients Not Candidates to Curative Previous Nefrectomy

SOGUG/0107
Start date: February 2008
Phase: Phase 2
Study type: Interventional

The purpose of this trial is to determinate the efficacy of Sunitinib in patients with renal cells carcinoma metastasic or locally avanced in patints not candidates to inicial curative nefrectomy.

NCT ID: NCT00663260 Completed - Clinical trials for Diabetes Mellitus, Type 2

Glycemic Efficacy and Renal Safety Study of Dapagliflozin in Subjects With Type 2 Diabetes Mellitus and Moderate Renal Impairment

Start date: June 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether dapagliflozin is effective in the treatment of type 2 diabetes in subjects with poor blood sugar control and moderate renal impairment

NCT ID: NCT00663052 Completed - Psoriasis Clinical Trials

Study Evaluating Etanercept for the Treatment of Moderate to Severe Psoriasis

PRISTINE
Start date: June 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the safety and efficacy of different doses of etanercept for the treatment of moderate to severe psoriasis.

NCT ID: NCT00662948 Completed - Lymphoma Clinical Trials

ZAR2007: R-CHOP in Folicular Lymphoma Patients no Treated Previously. Consolidation With 90Y Ibritumomab Tiuxetan (Zevalin®) Versus Maintenance Treatment With Rituximab (MabThera®)

Start date: December 2008
Phase: Phase 2
Study type: Interventional

After conventional induction treatment with R-CHOP (Rituximab, cyclophosphamide, adriamycin, vincristine and prednisone) the patients are randomized to: A: Consolidation with one dose of 90Y Ibritumomab tiuxetan (Zevalin®) 0,4 mCi/Kg B: Maintenance with 375 mg/m2 of Rituximab every 8 weeks during 24 months

NCT ID: NCT00662831 Completed - Diabetic Foot Ulcer Clinical Trials

Study Of The Effect Of Fragmin In The Treatment Of Neuroischaemic Foot Ulcers In Diabetic Patients

FEENICS
Start date: April 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of the study isto see the effect of Fragmin on the healing of diabetic foot ulcers by determining the number of subjects with ≥50% reduction in ulcer surface area including intact skin healing.

NCT ID: NCT00662701 Completed - Atrial Fibrillation Clinical Trials

Ablation or Surgery for Atrial Fibrillation (AF) Treatment

FAST
Start date: May 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to compare 2 invasive strategies for Atrial Fibrillation treatment, Endocardial catheter ablation isolation of the Pulmonary veins versus minimally invasive thoracoscopic surgical epicardial isolation. Both strategies are in use for several years now, and have been reported as a successful strategy with success rates of 60-90%. However, it is not known which technique is preferable in a given patient population in terms of efficacy to cure AF, safety, or patient discomfort. Therefore, in the present trial a randomized study is proposed to provide more insight into the relative merits of both techniques

NCT ID: NCT00661778 Completed - Clinical trials for Non-small Cell Lung Cancer

A Study of Avastin (Bevacizumab) in Combination With Docetaxel and Cisplatin in Patients With Metastatic or Locally Advanced Non-small Cell Lung Cancer

Start date: July 2007
Phase: Phase 2
Study type: Interventional

This study assessed the efficacy and safety of Avastin in combination with docetaxel and cisplatin as first-line treatment of patients with metastatic or locally advanced non-small cell lung cancer. Patients received Avastin 15 mg/kg intravenously (IV), docetaxel 75 mg/m^2, and cisplatin 75 mg/m^2 on Day 1 of each 3-week cycle for a maximum of 6 cycles.

NCT ID: NCT00661609 Completed - Bladder Cancer Clinical Trials

A Phase II Study of AZD4877 (a Novel Anti-mitotic Agent) in Advanced Bladder Cancer

Start date: May 2008
Phase: Phase 2
Study type: Interventional

The purpose of this Phase II study is to determine if AZD4877, an experimental drug that is a novel anti-mitotic agent (Eg5 or Kinesin Spindle Protein inhibitor that interferes with tumor cell division leading to tumor growth), can reduce tumor sizes in patients with bladder cancer