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Adverse Drug Event clinical trials

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NCT ID: NCT02559960 Suspended - Adverse Drug Event Clinical Trials

Post-marketing Safety Surveillance of Breviscapine Powder-Injection : a Registry Study

Start date: September 2015
Phase:
Study type: Observational

This registry aims to monitor the safety of Breviscapine Powder-Injection and to identify the potential risk factors for the adverse drug reactions.

NCT ID: NCT02413957 Completed - Elderly Clinical Trials

Medication Reconciliation in Comparison to an Extensive Medication Safety Check

Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine wether an extensive medication safety check has a greater impact on the incidence of adverse drug events than medication reconciliation or no intervention.

NCT ID: NCT02324803 Unknown status - Clinical trials for Carcinoma, Renal Cell

Phase II Study of Pazopanib as Second-line Treatment After Sunitinib in mRCC Patients

Start date: July 2014
Phase: Phase 2
Study type: Interventional

assess the activity and toxicity of second-line treatment with pazopanib after failure of first-line sunitinib treatment in patients with clear cell mRCC; to investigate the potential association of DLL4, Notch1, VEGFA, PDGFRB, HIF-1α and HIF-2α with clinical response to pazopanib in mRCC patients.

NCT ID: NCT02162147 Completed - Adverse Drug Event Clinical Trials

How Safe Are Our Pediatric Emergency Departments?

Start date: November 2014
Phase: N/A
Study type: Observational

Patient safety is an internationally recognized health care priority. Canadian data suggests that about 8% of adults admitted to hospital experience unintended harm (or 'adverse events') from the health care provided during their hospital stay. On a national level, this represents almost 25,000 preventable deaths among hospitalized adults each year. The emergency department is recognized as a high-risk environment for adverse events but most patient safety research is not specific to the emergency department. As well, the vast majority of people treated in the emergency department are sent home after their visit; yet safety research focuses primarily on people who are admitted to hospital. Finally, although children have also been identified as particularly high risk for suffering adverse events, very little research has been done on how often these events occur among children who visit the emergency department. Our study will address this gap in our knowledge about patient safety and provide important information on the frequency, severity and preventability of adverse events occurring among children in the emergency department. This information will help us to improve the safety of emergency department care for all Canadian children.

NCT ID: NCT02136017 Completed - Influenza Clinical Trials

Post-License Safety Evaluation of Influenza Virus Vaccine

Start date: January 2013
Phase: N/A
Study type: Observational

To evaluate the safety of the post-licensed influenza virus vaccine made of Changchun Institute of Biological Products Co.,Ltd.

NCT ID: NCT01897870 Completed - Patient Compliance Clinical Trials

The Effect of a Pharmacist Home Visit on Drug-related Problems Post-discharge.

HomeCoMe
Start date: November 2013
Phase: N/A
Study type: Interventional

the purpose of this study is to determine the the effect of a home-based medication management program on drug-related problems post-discharge.

NCT ID: NCT01080547 Completed - Quality of Life Clinical Trials

Study Comparing Conventional and Fast Track Multi-Discipline Treatment Interventions for Colorectal Cancer

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

A new notion"Fast Track Multi-Discipline Treatment" for colorectal cancer is thought with several benefits such as shorter hospitalization stay and less costs. This randomized study aims to compare the differences between conventional and Fast Track Multi-Discipline Treatment for colorectal cancer in hospitalization day, complications, costs and quality of life.

NCT ID: NCT00140504 Completed - Adverse Drug Event Clinical Trials

Preventing Adverse Drug Events With PatientSite

Start date: April 2003
Phase: N/A
Study type: Interventional

This is a study to better understand the nature and extent of adverse drug events (ADEs), defined as injuries due to prescription medications, in primary care. We will study whether PatientSite (an internet-based communication program for patients and health care providers) can improve clinicians' ability to detect adverse drug events among primary care patients and to mitigate the consequences by sending electronic queries to patients after they receive new medication prescriptions.