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NCT ID: NCT01048034 Completed - Clinical trials for Myelodysplastic Syndrome

Evaluation of Azacitidine in Transfusion Dependent Patients With Low-risk Myelodysplastic Syndrome (MDS) or Chronic Myelomonocytic Leukemia (CMML)

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

Azacitidine has proved prolonged overall survival in patients with high-risk MDS. Minor pilot studies have shown that treatment with Azacitidine can induce transfusion independency in previous transfusion dependent patients with low-risk MDS. This study will evaluate the effect of Azacitidine in transfusion dependent patients with low-risk MDS (IPSS low or int-1) or low risk CMML. Included patients should first have failed, or considered not being eligible to, treatment with EPO +/- G-CSF. Our hypothesis is that Azacitidine can lead to transfusion independency in this group of patients. Those patients who do not respond to treatment with Azacitidine alone, will be given treatment with the combination of Azacitidine and EPO where our hypothesis is that Azacitidine can restore sensitivity to EPO.

NCT ID: NCT01047839 Completed - Encephalitis Clinical Trials

Immunogenicity and Safety of the Japanese Encephalitis Vaccine IC51 (IXIARO®, JESPECT®) in a Pediatric Population in Non-endemic Countries

Start date: January 2010
Phase: Phase 3
Study type: Interventional

The primary objective is to assess the safety profile of IC51 in a pediatric population from regions where JEV is not endemic

NCT ID: NCT01047683 Completed - Clinical trials for Hypertriglyceridemia

Efficacy and Safety of AMR101 (Ethyl Icosapentate) in Patients With Fasting Triglyceride (Tg) Levels ≥ 500 and ≤ 2000 mg/dL

MARINE
Start date: December 2009
Phase: Phase 3
Study type: Interventional

The primary objective is to determine the efficacy of AMR101 (ethyl icosapentate) compared to placebo in lowering fasting triglyceride levels in patients with very high fasting triglyceride levels ≥ 500 and ≤ 2000 mg/dL.

NCT ID: NCT01047371 Completed - Pain Clinical Trials

Why in Hospital - Factors Determining Time to Discharge Readiness After Arthroplasty Surgery

Start date: January 2010
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate patient related factors determining length of stay in hospital after arthroplasty surgery.

NCT ID: NCT01047241 Completed - Pain Clinical Trials

Nasal Administration of Sufentanil+Ketamine for Procedure-related Pain in Children

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

The aim of the study is to investigate the absorption and clinical effect of nasal administration of an analgesic nasal spray containing sufentanil+ketamine for pain related to medical procedures in hospitalized children.

NCT ID: NCT01046838 Completed - Clinical trials for Heart Failure, Diastolic

SIDAMI - Sildenafil and Diastolic Dysfunction After Acute Myocardial Infarction (AMI)

SIDAMI
Start date: December 2009
Phase: Phase 4
Study type: Interventional

In patients with Doppler echocardiographic signs of elevated LV filling pressures despite preserved LV systolic function after AMI treatment with the phosphodiesterase inhibitor sildenafil 40 mg three times daily for 9 weeks will compared with placebo 1. Improve resting LV filling and cardiac hemodynamics. 2. Improve exercise capacity. 3. Improve filling pattern and cardiac hemodynamics during exercise.

NCT ID: NCT01046071 Completed - Clinical trials for Laparoscopic Cholecystectomy

The Analgesic Efficacy of Transversus Abdominis Plane Block After Laparoscopic Cholecystectomy

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

The purpose of this study is to determine whether Transversus abdominis plane block as part of a multimodal postoperative regimen is superior to control in analgesic efficacy after laparoscopic cholecystectomy.

NCT ID: NCT01045603 Completed - Clinical trials for Breakthrough Cancer Pain

Instanyl® Non-Interventional Study

INIS
Start date: December 2009
Phase: N/A
Study type: Observational

The aim of this study is to describe the use of Instanyl® (Intranasal fentanyl spray) in the treatment of breakthrough pain (BTP) in cancer patients by success of dose titration and distribution of dose strength. Data will be collected at three different time points over a 3 month period.

NCT ID: NCT01043445 Completed - Type 2 Diabetes Clinical Trials

-Oleoyl Glycerol is a GPR119 Agonist and Signals GLP-1 Release in Humans.

Start date: September 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the impact of different ligands of GPR 119 (a G protein-coupled receptor in the intestine) on the secretion of the incretin hormones, GLP-1 and GIP.

NCT ID: NCT01042769 Completed - Clinical trials for Diabetes Mellitus Type 2

A Study With Aleglitazar in Patients With a Recent Acute Coronary Syndrome and Type 2 Diabetes Mellitus

Start date: February 2010
Phase: Phase 3
Study type: Interventional

This double-blind, parallel, two-arm study will evaluate the potential to reduce cardiovascular risk, the tolerability and long-term safety profile of aleglitazar compared to placebo on top of standard care in patients with recent acute coronary syndrome (ACS) and type 2 diabetes mellitus. Patients will be randomized to receive either aleglitazar or placebo once daily as oral doses. The study will last until at least 950 events occur, but time on study treatment will be for at least 2.5 years.