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NCT ID: NCT00739739 Completed - Clinical trials for Interstitial Cystitis

An Effectiveness And Safety Study Of PD 0299685 For The Treatment Of Symptoms Associated With Interstitial Cystitis

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

The purpose of this study is to determine whether PD 0299685 is effective in the treatment of symptoms associated with interstitial cystitis/painful bladder syndrome, such as pain, urinary urgency and frequency. At the same time assess the drug's safety and tolerability.

NCT ID: NCT00738894 Completed - Stroke Clinical Trials

GORE® Septal Occluder Device for Patent Foramen Ovale (PFO) Closure in Stroke Patients

REDUCE
Start date: December 10, 2008
Phase: N/A
Study type: Interventional

The primary objective is to determine if patent foramen ovale (PFO) closure with the GORE® HELEX® Septal Occluder or GORE® CARDIOFORM Septal Occluder plus antiplatelet medical management is safe and effective and reduces the risk of recurrent stroke or imaging-confirmed transient ischemic attack (TIA) when compared to antiplatelet medical management alone in patients with a PFO and history of cryptogenic stroke or imaging-confirmed TIA. A co-primary objective is to demonstrate that medical management plus closure with the study device reduces the risk of new brain infarct compared to medical management alone.

NCT ID: NCT00738816 Completed - Elderly Clinical Trials

Effect of Systematic Medication Review in Elderly Patients Admitted to an Orthopedic Department

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

Elderly patients have a higher risk of experiencing adverse drug events due to an age related increase in morbidity and medication use. Inappropriate or wrong medication use among elderly patients acutely admitted to hospitals is assumed to result in earlier contact to general practitioner, emergency departments and re-admissions if not corrected during hospital admission. It is therefore our hypothesis that a systematic medication review conducted by pharmacists and physicians specialized in pharmacology will increase time to first unscheduled physician contact (general practitioner, emergency departments, ambulatory care and re-admissions) after discharge from hospital from an average of 21days to 25 days. Further, the following secondary outcome parameters will be measured at discharge and within 3-month follow-up: - length of in-hospital stay - number of contacts to general practitioner 30 days after discharge, that resulted in medication changes - number of re-admissions at 3-month - number of death at 3-month - number of contact to primary health care at 3-month - patients self-experienced quality of health(EQ-5D) 3-month

NCT ID: NCT00738166 Completed - Healthy Clinical Trials

Content, Bioavailability and Health Effects of Trace Elements and Bioactive Components in Organic Agricultural Systems

OrgTrace
Start date: October 2007
Phase: N/A
Study type: Interventional

Trace elements, bioactive secondary metabolites and vitamins are among the most important quality parameters in plants. Yet, very little information is available on their content, bioavailability and health effects of organically grown plant food products. The main objective of the project is to study the impact of different agricultural management practises relevant for organic farming on the ability of cereal and vegetable crops to absorb trace elements from the soil and to synthesise bioactive compounds (secondary metabolites, antioxidant vitamins and phytates) with health promoting effects. Field experiments with a rigidly controlled design will be implemented together with state-of-the-art analytical techniques allowing solid conclusions to be drawn on the variability and optimum levels of bioactive compounds. The multitude of analytical data from plant and soil samples will be analysed by multivariate statistical methods in order to reveal differences between the cultivation systems used. Finally, the relationship between bioavailability of the nutrients studied and the elemental fingerprint of plants will be extracted by the statistical methods.

NCT ID: NCT00736489 Completed - Asthma Clinical Trials

Single-dose Crossover Study to Investigate Pharmacodynamics of AZD3199

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

The purpose of this study is to investigate the pharmacodynamics of single doses of AZD3199 in asthmatic patients.

NCT ID: NCT00736138 Completed - Arthritis of Knee Clinical Trials

Hyperpronation and Foot Pain

Start date: June 2007
Phase: N/A
Study type: Interventional

Effects of training and pellots

NCT ID: NCT00735813 Completed - Neoplasms Clinical Trials

Taurolidine Lock Solution in the Prevention of Catheter Related Bacteremia

Start date: April 2008
Phase: Phase 3
Study type: Interventional

Children with cancer need a long term tunnelled central venous catheter (TCVC) for the entire duration of their treatment. TCVCs are locked with heparin when not in use. The most frequent complications of long term TCVC are catheter related blood steam infections. Taurolock is a new lock that is claimed to prevent the formation of luminal biofilm in TCVCs and has been demonstrated to eradicate infected CVCs. In this study the investigators will compare TCVCs locked with heparin with TCVCs locked with Taurolock. Hypothesis: Taurolock will diminish the number of CRBSI in children with cancer compared with children with heparin lock of their CVC.

NCT ID: NCT00735501 Completed - Clinical trials for Diabetes Mellitus, Type 2

Observational Study to Observe the Safety of Levemir® Treatment in Patients With Type 2 Diabetes

Start date: March 2008
Phase: N/A
Study type: Observational

This observational study is conducted in Europe. The study aims to observe the incidence of serious adverse drug reactions in subjects with type 2 diabetes during Levemir® treatment.

NCT ID: NCT00734591 Completed - Diabetes Mellitus Clinical Trials

Follow-Up Study for Exubera

FUSE
Start date: August 2008
Phase: N/A
Study type: Observational

In studies of Exubera in persons with diabetes, lung cancer occurred in a few more people who were taking Exubera than in people who were taking other diabetes medicines. All subjects diagnosed with lung cancer had a history of smoking and the number of lung cancer cases observed fell within the expected range based on population-based data. There is currently not enough information to determine if any of the observed lung cancer cases were related to Exubera use, therefore, the study is being conducted to further investigate whether Exubera use makes the appearance of lung cancer more likely.

NCT ID: NCT00733343 Completed - Heart Failure Clinical Trials

Treatment of Predominant Central Sleep Apnoea by Adaptive Servo Ventilation in Patients With Heart Failure

Serve-HF
Start date: February 2008
Phase: N/A
Study type: Interventional

The purpose of this trial is to evaluate the long-term effects and cost-effectiveness of adaptive servo-ventilation (ASV) on the mortality and morbidity of patients with stable heart failure due to left ventricular systolic dysfunction, already receiving optimal medical therapy, who have sleep disordered breathing (SDB) that is predominantly central sleep apnea. Assumptions: the intervention reduces the hazard rate by 20%. The event rate in the control group is 35% in the first year. It is assumed that the hazard rate is constant over time.