Clinical Trials on Adverse Event

Total 2124 results

University of Pittsburgh
RAND

Completed

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

Adverse Drug Events

United States
US Department of Veterans Affairs

Completed

Patient Profiling and Provider Feedback to Reduce Adverse Drug Events

Adverse Drug Events

United States
Westview Physician Collaborative

Completed

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

Adverse Drug Events

Canada
Ottawa Hospital Research Institute
McGill University; Canadian Institutes of Health Research (CIHR)

Completed

Information Systems-enabled Outreach Program for Adverse Drug Events (ISTOP-ADE)

Adverse Drug Events

Canada
Intermountain Health Care, Inc.

Completed

Response to Medication Registry

Adverse Drug Events

United States
Cedars-Sinai Medical Center
National Institutes of Health (NIH); National Institute on Aging (NIA)

Completed

Pharmacists and Pharmacy Technicians to Improve Admission Medication History Accuracy

Adverse Drug Events
University of Massachusetts, Worcester
Agency for Healthcare Research and Quality (AHRQ); Baycrest Centre for Geriatric...

Withdrawn

Reducing Adverse Drug Events in the Nursing Home

Adverse Drug Events
Indiana University
Brigham and Women's Hospital

Completed

Improving Safety by Basic Computerizing Outpatient Prescribing

Adverse Drug Events

United States
Sultan Qaboos University

Completed

Impact of Medication Reconciliation Intervention on the Rate of Preventable Adverse Drug Events (ADEs) and Healthcare Utilization

Adverse Drug Events
VA Office of Research and Development

Completed

Implementation of Real-time ADE Surveillance and Decision Support (VA ADE)

Adverse Drug Events

United States
University of Massachusetts, Worcester
Agency for Healthcare Research and Quality (AHRQ); Qualidigm

Completed

Enhancing the Safety of Warfarin in Nursing Homes

Adverse Drug Events (ADEs)

United States
McGill University
Canadian Institutes of Health Research (CIHR)

Completed

Using Novel Canadian Resources to Improve Medication Reconciliation at Discharge

Adverse Drug Events | Medication Reconciliation

Canada
Brigham and Women's Hospital
University of Chicago; University of Wisconsin, Madison; University of California... and other collaborators

Completed

Multi-Center Medication Reconciliation Quality Improvement Study (MARQUIS)

Medication Administered in Error | Adverse Drug Events

United States
Brigham and Women's Hospital

Unknown

Ambulatory Medication Reconciliation Following Hospital Discharge

Medication Administered in Error | Adverse Drug Events

United States
University Hospital, Montpellier

Completed

Drug-Related Problems : Focus on Age and Diabetes (DRP-AD)

Adverse Drug Events

France
Xuanwu Hospital, Beijing

Unknown

Safety and Efficacy of Distal Embolic Protection Device in Vertebral Artery Origin Stenting

Adverse Event

China
Nantes University Hospital
Université de Nantes

Not yet recruiting

Patient Safety Incidents in Coordinated Primary Care Teams: a Multi-method Study (EVIDENS-Prim)

Adverse Event
Université du Québec à Trois-Rivières

Completed

Adverse Events Associated With Manual Therapies in Children

Adverse Event

Canada
Hospices Civils de Lyon

Unknown

Impact on the Adverse Event (AE) Incidence of Two Types of Experience Feedback on AE Analyzed During Local Morbidity Mortality Reviews (RMM Simulation)

Hospital Adverse Event

France
Universidad Miguel Hernandez de Elche
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la...

Active, not recruiting

Gender Bias in the Overuse Studies Conducting in Primary Care (OVERGEND)

Severe Adverse Event

Spain
Lucie Heinzerling

Recruiting

Treatment of Immune-related Adverse Events Refractory to Standard Therapy and Associated Changes in Immunophenotype (PRIA)

Immune-related Adverse Event

Germany
Chang Gung Memorial Hospital
Ministry of Science and Technology, Taiwan

Recruiting

Hyperpolarized 13C-MRI and Metabolomics for Immune-related Adverse Events (DNP_irAE)

Immune-related Adverse Event

Taiwan
University of Rochester
Agency for Healthcare Research and Quality (AHRQ)

Completed

Emergency Pharmacist Safety Study

Adverse Drug Event, Potential Adverse Drug Event, and Quality Measures

United States
Duke University

Enrolling by invitation

Immune-Related Adverse Events and Associated Biomarkers in Patients Receiving Cancer Immunotherapy (IMBARC)

Cancer | Immune-related Adverse Event

United States
Helse Stavanger HF

Completed

Endothelial Function and Heart Rate Variability After Stenting (FUNKIS)

Restenosis or Adverse Cardiovascular Event

Norway
Universitair Ziekenhuis Brussel

Recruiting

Food Intervention to Reduce Immunotherapy toXicity (FORX01)

Dietary Habits | Immune-related Adverse Event

Belgium
University of Alberta

Completed

Comparison of Active vs. Passive Surveillance to Collect Adverse Events

Adverse Events

Canada
Irrimax Corporation

Completed

Retrospective Independent Safety Review of Closed Irrisept Study

Adverse Events

United States
Northwestern University
University of Michigan; The University of Texas Health Science Center at San... and other collaborators

Completed

Redesigning Systems to Improve Quality for Hospitalized Patients (RESET)

Interdisciplinary Communication | Adverse Event | Interprofessional Relations | Interpersonal Relations

United States
AstraZeneca

Completed

Study to Compare the Bioavailability of ABT-335 and Rosuvastatin From ABT-143 Relative to That From the Co-administration of ABT-335 and Rosuvastatin Calcium

Adverse Events | Pharmacokinetic

United States
Brigham and Women's Hospital
Crico

Completed

PREventing Adverse Events Post-Discharge Through Proactive Identification, Multidisciplinary Communication, and Technology (PREDICT)

Adverse Event | Transitions of Care | General Medicine | Discharge Checklist

United States
University of Sao Paulo General Hospital

Completed

Adverse Events During Physiotherapy at Intensive Care Unit In Patients Undergoing Cardiac Surgery (Adephysio)

Cardiac Surgery | Physiotherapy | Adverse Event | Intensive Care Units | Postoperative
Zhong Wang
Shanxi Zhendong Pharmacy Co., Ltd

Recruiting

Post-marketing Safety Surveillance of Qizhi Tongluo Capsules:a Registry Study.

Adverse Drug Events | Adverse Drug Reactions | Severe Adverse Events | Safety Surveillance | Severe Adverse Reactions

China
Zhong Wang
Shanxi Zhendong pharmaceutical Co. LTD.

Completed

Post-marketing Safety Surveillance of Compound Kuh-seng Injection: a Registry Study

Adverse Drug Events | Adverse Drug Reactions | Severe Adverse Events | Safety Surveillance | Severe Adverse Reactions

China
Sichuan Provincial People's Hospital

Recruiting

Risk Factors and Risk Grading Prediction of Perioperative Respiratory Adverse Events in Children

Perioperative Respiratory Adverse Events

China
AstraZeneca

Completed

Study to Compare the Bioavailability of ABT-335 and Rosuvastatin From ABT-143 Capsules Relative to That From Co-administration of ABT-335 and Rosuvastatin for the 5/45mg Dosage Form.

Adverse Events | Pharmacokinetic Variables

United States
Insel Gruppe AG, University Hospital Bern
The Hospital for Sick Children; Children's Hospital of Philadelphia; Charite... and other collaborators

Recruiting

CRICKET: Critical Events in Anaesthetised Kids Undergoing Tracheal Intubation (CRICKET)

Intubation Complication | Adverse Events

United States, Australia, Canada, Germany, Switzerland
Centre Hospitalier Universitaire, Amiens
Central Hospital Saint Quentin

Recruiting

Identification of Predictive Biomarkers for Immune-Related Adverse Events (irAEs) in Patients Undergoing Immune CheckPoint Inhibitors (ICPI) Treatment (Ibe2i-TIPCI)

Immunotherapy | Immune Checkpoint Inhibitors | Immune-related Adverse Event | Predictive Biomarkers

France
Institut Mutualiste Montsouris

Recruiting

Fast-Track Cardiovascular Assessment for Suspicion of Cardiovascular Events on Immunecheckpoint Inhibitors (FAST-TRACK)

Cancer | Cardiovascular Complication | Immune Checkpoint Inhibitor | Immune-related Adverse Event

France
Bamrasnaradura Infectious Diseases Institute

Completed

Nevirapine Levels and Fluconazole

Adverse Event | Nevirapine | Fluconazole
Pierre Van Damme

Completed

A Study to Assess the Acceptability and Usability of a New Device for Intradermal Vaccination

Pain | Vaccination Adverse Event

Belgium
University of British Columbia
Canadian Institutes of Health Research (CIHR); Vancouver Coastal Health; Ministry...

Not yet recruiting

Evaluating ActionADE in Reducing Adverse Drug Reactions

Adverse Drug Event | Adverse Drug Reaction
University Medical Center Groningen

Recruiting

Adverse Event Prediction in Geriatric Patients in the ED With Ultrasound (AGEDU)

Frailty | Adverse Event

Netherlands
Institute for Clinical Effectiveness and Health...
Ministry of Public Health, Argentina; Hospital JP Garrahan

Completed

Reducing Adverse Events in Pediatric Intensive Care Units in Argentina

Medical Errors | Preventable Adverse Events

Argentina
St. Justine's Hospital
CIUSSS du Nord-de-l'Île-de-Montréal

Recruiting

Monitoring of Metabolic Adverse Events of Second Generation Antipsychotics in a Naive Pediatric Population (MEMAS)

Adverse Drug Event

Canada
Assistance Publique - Hôpitaux de Paris
Institut National de la Santé Et de la Recherche Médicale, France

Completed

Medication Reconciliation Using Electronic Pharmaceutical Record: A Multicenter Study in the Hospitalized Elderly (CONCIPAGE)

Adverse Drug Event

France
Brigham and Women's Hospital
National Institutes of Health (NIH); Atrius Health

Completed

Optimizing Electronic Health Record Prompts With Behavioral Economics to Improve Prescribing for Older Adults (NUDGE-EHR)

Aging | Adverse Drug Event | Benzodiazepine Sedative Adverse Reaction | Anticholinergic Adverse Reaction

United States
Michigan State University
University of Wisconsin, Madison

Completed

Over-the-counter (OTC) Labels for Older Adults

Adverse Drug Event

United States
KK Women's and Children's Hospital

Completed

Ametop - Friend and Foe A Prospective Study of the Incidence of Adverse Reactions With Ametop

Adverse Drug Event
Dana-Farber Cancer Institute
Beth Israel Deaconess Medical Center; Blue Cross Blue Shield; Agency for Healthcare...

Completed

Preventing Adverse Drug Events With PatientSite

Adverse Drug Event

United States

Clinical Trials on Adverse Event

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CROs in United Arab Emirates

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