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NCT ID: NCT00900822 Completed - Alveolar Bone Loss Clinical Trials

Straumann Bone Ceramic Versus BioOss in Sinus Elevation

Start date: November 2005
Phase: N/A
Study type: Interventional

Straumann Bone Ceramic (SBC) and BioOss will be used as bone grafting materials when there is a need for bone augmentation in the posterior upper jaw. 9 months later the bone formation is evaluated. The patients are followed for 3 years.The study hypothesis is that the SBC is not worse than BioOss.

NCT ID: NCT00900627 Completed - Breast Cancer Clinical Trials

Phase I/II AZD8931/Paclitaxel in Treatment of Advanced Solid Tumours (Phase I) and Advanced Breast Cancer (Phase II)

THYME
Start date: June 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The main purpose of this study is to determine if AZD8931 can improve the efficacy of standard chemotherapy for the treatment of advanced breast cancer. This study will be conducted in 2 parts: the first part (phase I) will determine a dose of AZD8931 that can be safely administered with paclitaxel chemotherapy. The second part (phase II) will determine the efficacy and safety of AZD8931 in combination with paclitaxel chemotherapy in breast cancer.

NCT ID: NCT00900614 Completed - Prostatic Neoplasms Clinical Trials

Safety Study of APR-246 in Patients With Refractory Hematologic Cancer or Prostate Cancer

Start date: May 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the highest feasible dose (HFD) of intravenous (IV) APR-246 when given to patients with refractory hematologic malignancies or prostate carcinoma.

NCT ID: NCT00895674 Completed - Clinical trials for Carcinoma, Renal Cell

Patient Characteristics in Advanced Renal Cell Carcinoma and Daily Practice Treatment With Nexavar

Start date: July 2006
Phase: N/A
Study type: Observational

Renal cell carcinoma accounts for roughly 3 % of all cancer. It is a rather aggressive cancer type, which means that patients who present with an advanced disease have a rather poor prognosis. When this study has been started the standard therapy for patients has been cytokines, which might be accompanied by significant toxicities or might fail the therapeutic goal. In these cases sorafenib can be a feasible therapeutic option. This non-interventional study has been created and is being conducted to collect clinical data on the patients' therapy with sorafenib in an everyday treatment schedule. The main goal of this study focuses on patient characteristics and tumor status in RCC treated with sorafenib as well as the treatment duration and safety of sorafenib under everyday treatment conditions.

NCT ID: NCT00894816 Completed - Obesity Clinical Trials

Probiotics in Prevention of Allergies, Obesity and Caries

ELEFANT
Start date: August 2000
Phase: N/A
Study type: Interventional

During the period of 2000-2003, 179 healthy, term infants with no previous signs of allergic disease were recruited and randomized to daily intake of cereals with or without the addition of Lactobacillus paracasei subspecies paracasei strain F19 (LF19) from 4-13 months of age. The effects of LF19 on gut microbial composition, infections, allergies, immunological development, growth and blood lipids were monitored. Of 179 included infants, 171 completed the study. The study product was well tolerated with no observed side effects. Compliance was excellent. In a follow-up study, the aim is to investigate the long-term effects of feeding LF19 during weaning on allergies, immune programming, overweight, gut microbial composition and oral health in 8-year old children. The investigators' primary outcome will be to determine whether daily intake of LF19 during weaning results in less eczema at 8 years of age, and if the preventive effect encompasses also respiratory allergies and immunoglobulin E (IgE) - sensitization. The long term effects on gut microbial composition, overweight and metabolic markers will be investigated. Furthermore, the possible preventive effects of LF19 on caries will be assessed.

NCT ID: NCT00894595 Completed - Knee Injury Clinical Trials

Preventing Knee Injuries in Adolescent Female Football Players

Start date: August 2008
Phase: N/A
Study type: Interventional

Football-related knee injuries are common and especially the anterior cruciate ligament (ACL) injury constitute a serious problem in football regardless of the playing level. The purpose of this study is to conduct a randomized controlled trial evaluating the effect of a training program designed to prevent acute knee injury in female adolescent football players. The investigators' hypotheses are: 1. a preventive training program reduces the incidence of ACL injury, and 2. a high match frequency and match play at senior level increase the risk of ACL injury.

NCT ID: NCT00894387 Completed - Clinical trials for Congestive Heart Failure

Six Months Efficacy and Safety of Aliskiren Therapy on Top of Standard Therapy, on Morbidity and Mortality in Patients With Acute Decompensated Heart Failure

ASTRONAUT
Start date: May 2009
Phase: Phase 3
Study type: Interventional

This study evaluated the effect of early initiation of aliskiren therapy, compared to standard therapy, in the reduction of cardiovascular death and heart failure re-hospitalization events within 6 months, in congestive heart failure (CHF) patients hospitalized for an episode of acute decompensated heart failure.

NCT ID: NCT00893451 Completed - Insulin Resistance Clinical Trials

Study of Vitamin D3 Supplementation in Patients With Chronic Kidney Disease

VitaD-CKD1
Start date: September 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the impact of vitamin D3 supplementation on the insulin resistance in non-diabetic patients with chronic kidney disease (CKD) stages 3-4, vitamin D deficiency/insufficiency and elevated fasting serum insulin levels.

NCT ID: NCT00892944 Completed - Healthy Clinical Trials

An Open Label Positron Emission Tomography (PET) Study to Determine Central mGluR5 Receptor Occupancy of AZD2516

Start date: April 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine if AZD2516 binds to mGluR5 receptors in the brain. This will then help to make accurate predictions of efficacy and dosing in the future development programme.

NCT ID: NCT00892840 Completed - Depression Clinical Trials

Multiple-Ascending Dose Study

Start date: May 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety and tolerability of BMS-820836 after multiple doses