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NCT ID: NCT00792402 Completed - Clinical trials for Chronic Heart Failure

Computerized Guideline in Heart Failure: Implementation Process and Impact Evaluation

Start date: November 2007
Phase: N/A
Study type: Observational

Objective: To assess the effectiveness of implementation process of an electronic Heart Failure guideline in primary care in the city of Barcelona.

NCT ID: NCT00791778 Completed - Ovarian Neoplasms Clinical Trials

Comparison of Nexavar/Placebo as Maintenance Therapy for Patients With Advanced Ovarian or Primary Peritoneal Cancer

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

Comparison of Nexavar with a placebo as maintenance therapy for patients with advanced Ovarian or primary Peritoneal cancers in complete remission following surgery and one regimen of chemotherapy.

NCT ID: NCT00791739 Completed - Fibromyalgia Clinical Trials

Trazodone and Its Augmentation With Pregabalin in the Treatment of Fibromyalgia

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

The study has a double purpose: a first phase intends to assess the effectiveness and tolerability of trazodone, an antidepressant with sedative and sleep-promoting properties, in the treatment of fibromyalgia; a second phase intends to evaluate if the addition of pregabalin to patients who have shown a partial response to trazodone additionally improves fibromyalgia symptomatology.

NCT ID: NCT00791687 Completed - Oxidative Stress Clinical Trials

Prenatal Corticosteroids and Antioxidants in Preterm Infants

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

Premature infants are highly susceptible to oxidative stress because of the immaturity of their antioxidant defense system. The use of prenatal glucocorticosteroids administered to the mother improves respiratory function and overall outcome. The investigators hypothesize that prenatal glucocorticosteroids favor the expression and competence of the antioxidant defense system.

NCT ID: NCT00791479 Completed - Clinical trials for Diabetes Mellitus, Type 2

Effects of LY2189265 on Glycemic Control in Participants With Type 2 Diabetes

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

This is a study to demonstrate that different doses of once-weekly LY2189265 injected subcutaneously will have dose proportional effect on hemoglobin A1c (HbA1c) at 12 weeks in participants with type 2 diabetes mellitus.

NCT ID: NCT00790920 Completed - Stroke Clinical Trials

Efficacy and Safety Study of Desmoteplase to Treat Acute Ischemic Stroke

DIAS-3
Start date: December 2008
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine whether desmoteplase is effective and safe in the treatment of patients with acute ischaemic stroke when given within 3-9 hours from onset of stroke symptoms.

NCT ID: NCT00790907 Completed - Clinical trials for Acute Coronary Syndrome

Fondaparinux Trial With Unfractionated Heparin (UFH) During Revascularization in Acute Coronary Syndromes (ACS)

FUTURA/OASIS 8
Start date: February 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the safety of two different dose regimens of unfractionated heparin (UFH) during a percutaneous coronary intervention (PCI) procedure in patients with UA (unstable angina)/NSTEMI (non ST segment elevation myocardial infarction) who have been initially treated with fondaparinux.

NCT ID: NCT00790816 Completed - Neoplasms, Breast Clinical Trials

Continuation Study of Lapatinib Monotherapy or Lapatinib in Combination With Other Anti-cancer Agents

Start date: October 2008
Phase: Phase 1
Study type: Interventional

This study is designed to provide continued access to lapatinib as monotherapy or as part of a combination regimen to cancer subjects who are currently participating in a phase I trial that has met its study objectives.

NCT ID: NCT00790426 Completed - Urothelial Cancer Clinical Trials

Phase II Study of TKI258 in Advanced Urothelial Carcinoma

Start date: March 2010
Phase: Phase 2
Study type: Interventional

This study will evaluate the efficacy of TKI258 in patients with advanced urothelial cancer

NCT ID: NCT00790400 Completed - Clinical trials for Lymphangioleiomyomatosis (LAM)

Efficacy and Safety of RAD001 in Patients Aged 18 and Over With Angiomyolipoma Associated With Either Tuberous Sclerosis Complex (TSC) or Sporadic Lymphangioleiomyomatosis (LAM)

EXIST-2
Start date: April 2009
Phase: Phase 3
Study type: Interventional

This study will evaluate the safety and efficacy of RAD001 in treating patients with Angiomyolipoma associated with Tuberous Sclerosis Complex or Sporadic Lymphangioleiomyomatosis.