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Adverse Drug Events clinical trials

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NCT ID: NCT01764204 Completed - Adverse Drug Events Clinical Trials

Hospital Intensive Monitoring of Adverse Drug Reactions of Qingkailing Injection In The Next Two Years

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

To highlight the incidence of adverse reactions of Qingkailing Injection.

NCT ID: NCT01531088 Completed - Adverse Drug Events Clinical Trials

Enhancing the Detection and Management of Adverse Drug Events in Nursing Homes

Start date: January 2012
Phase: N/A
Study type: Interventional

Adverse drug events (ADEs) are the most clinically significant and costly medication-related problems in nursing homes (NH) and are associated with an estimated 93,000 deaths a year and as much as $4 billion of excess healthcare expenditures. Current ADE detection and management strategies that rely on pharmacist retrospective chart reviews (i.e., usual care) are inadequate. Active medication monitoring systems are recommended by many safety organizations as an alternative to detect and manage ADEs. These systems have been shown to be less expensive, faster, and identify ADEs not normally detected by clinicians in the hospital setting. The investigators developed and pilot-tested an active medication monitoring system for use in a single NH, where it was shown to detect ADEs with a high degree of accuracy and at a rate of nearly 2.5 times that of usual care. The long-term objective of our proposed research is to improve patient safety with respect to medications in NHs. The short-term objectives or specific aims of our proposed research are to determine if NH patients managed by physicians who receive active medication monitoring alerts have more ADEs detected, have a faster ADE management response time, and can result in more cost-savings from a societal perspective compared to usual care.

NCT ID: NCT01337063 Completed - Adverse Drug Events Clinical Trials

Multi-Center Medication Reconciliation Quality Improvement Study

MARQUIS
Start date: March 2011
Phase: N/A
Study type: Interventional

Patients often have problems after they leave the hospital, in part because errors are made in the medications they are prescribed. The goal of this project is to develop a more accurate and safe medication prescription process when patients enter and leave the hospital and implement this process at six U.S. hospitals. The investigators will measure the success of the project and develop lessons learned so this process can be applied to other hospitals.

NCT ID: NCT01179867 Completed - Adverse Drug Events Clinical Trials

Using Novel Canadian Resources to Improve Medication Reconciliation at Discharge

Start date: October 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if a physician's use of electronic medication reconciliation software when writing a patient's discharge prescription will prevent adverse drug events and readmissions to the hospital. This electronic medication software will provide the physician with the most up-to-date list of medications the patient was taking before being admitted to the hospital, through a real-time link to the provincial drug insurance agency's administrative databases. It will also provide the list of medications the patient has taken while admitted to the hospital. With these two pieces of information, the physician will write the discharge prescription using the medication management software, print the discharge prescription for the patient, and the software will fax a copy of any prescriptions that should be stopped to the patient's community pharmacist.

NCT ID: NCT01164137 Completed - Adverse Drug Events Clinical Trials

Eliminating Risk of Preventable Adverse Drug Events at the Hospital-community Interface of Care

CMR
Start date: November 2008
Phase: N/A
Study type: Interventional

This initiative aims to decrease the risk of medication errors at the hospital-community interface as well as health system utilization following hospital discharge by implementing a pharmacist-led medication reconciliation in the patients' home within 72 hours of hospital discharge.

NCT ID: NCT01091038 Completed - Adverse Drug Events Clinical Trials

Improving Safety by Basic Computerizing Outpatient Prescribing

Start date: August 2001
Phase: Phase 2/Phase 3
Study type: Interventional

The study will measure the effect of basic clinical decision support on medical errors and adverse drug events in the ambulatory setting.

NCT ID: NCT00780572 Completed - Adverse Drug Events Clinical Trials

Implementation of Real-time ADE Surveillance and Decision Support

VA ADE
Start date: December 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if an electronic alerting technology improves time to intervention for possible ADEs, identify what factors affect adoption of ADE alerts, and whether there is a cost benefit associated with the alerting technology.

NCT ID: NCT00013143 Completed - Adverse Drug Events Clinical Trials

Patient Profiling and Provider Feedback to Reduce Adverse Drug Events

Start date: June 2001
Phase: N/A
Study type: Interventional

Adverse drug events (ADE) present a unique focus for error reduction. Computerized provider order entry, with embedded clinical decision support, has great promise in reducing medication errors but preventable adverse drug events may still occur despite such systems.