Search clinical trials for: Adverse drug events

Total 261980 results

Canadian Network for Observational Drug Effect...
Canadian Institutes of Health Research (CIHR); Drug Safety and Effectiveness...

Completed

Direct Oral Anticoagulants and Venous Thromboembolism

Venous Thromboembolism | Major Bleed

Canada
Vanderbilt University

Terminated

Tissue-Type Plasminogen Activator (t-PA) Release Predicts Major Adverse Cardiac Events (MACE) in Patients With Non-critical Coronary Artery Disease

Coronary Artery Disease

United States
AbbVie

Completed

Assessment of the Safety of ABT-308 in Healthy Volunteers and Subjects With Asthma

Asthma
University Hospital, Caen

Unknown

Residual Plasma Concentration of Sorafenib and Adverse Events in CHC (PharmacoCHC)

Advanced or Metastatic Hepatocellular Carcinoma

France
IMMUNOe Research Centers

Completed

The Benefit of 5% IVIG for Patients With Primary Immunodeficiency Disorders Who Experience Adverse Events on 10% IVIG Preparations

Primary Immunodeficiency
Bristol-Myers Squibb

Completed

Cost of Adverse Events Related to How Often Follow-Up Occurs Among Patients With Cancer That Has Spread

Melanoma

United States
National Institutes of Health Clinical Center (CC)

Completed

Drug Interaction Study Between Inhaled Beclomethasone and Protease Inhibitors in Healthy Volunteers

Asthma | HIV

United States
Baim Institute for Clinical Research
Bristol-Myers Squibb; Eli Lilly and Company; Daiichi Sankyo, Inc.; Boston Scientific... and other collaborators

Completed

The Dual Antiplatelet Therapy Study (DAPT Study)

Coronary Artery Disease

United States, Australia, Czechia, New Zealand, United Kingdom, Germany, Hungary, Poland, France, Romania
Zahra Vahdat Shariatpanahi

Completed

Comparison of Daily Single Dose Triple and Conventional Triple Therapies for Helicobacter Pylori Infection

Helicobacter Infection

Iran, Islamic Republic of
GlaxoSmithKline
The TIMI Study Group

Completed

A Phase 3 Clinical Outcomes Study to Compare the Incidence of Major Adverse Cardiovascular Events in Subjects Presenting With Acute Coronary Syndrome Treated With Losmapimod Compared to Placebo (LATITUDE-TIMI 60) (LATITUDE)

Acute Coronary Syndrome

United States, Australia, France, Spain, Taiwan, Estonia, Poland, Russian Federation, Belgium, Philippines, Sweden, Thailand, Germany, Israel, Bulgaria, Hong Kong, Netherlands, Norway, Slovakia, South Africa, Korea, Republic of, R... and more
University of Chile

Unknown

Impact of Clinical Pharmacist on Adverse Drug Events in Older Adults

Drug-Related Side Effects and Adverse Reactions

Chile
University of Roma La Sapienza

Completed

Safety, Immunogenicity And Efficacy Of Vaccination In Military Personnel

Vaccination Failure | Vaccination Adverse Events | Specific Antibody Response

Italy
University of California, Berkeley

Completed

Daily Irrigation With Silicone Hydrogel Contact Lens Continuous Wear (EW23)

Corneal Epithelial Permeability
University of Alabama at Birmingham

Completed

Fast Track CSII Using a Novel Device in Young Children With Newly Diagnosed T1DM

Type 1 Diabetes Mellitus

United States
Merck Sharp & Dohme LLC
AESCA Pharma GmbH

Terminated

Induction of Remission in RA Patients at Low Disease Activity by Additional Infliximab Therapy (Study P04644AM1) (TERMINATED)

Rheumatoid Arthritis
Intermountain Health Care, Inc.

Completed

Methadone Monitoring for Insights Into Adverse Events (MEMORIES)

Pain | Opiate Addiction

United States
Royal College of Anesthesiologists of Thailand
Chulalongkorn University; Khon Kaen University; Ramathibodi Hospital; Prince of... and other collaborators

Completed

The Thai Surgical Intensive Care Study (Thai-SICU Study) (THAI-SICU)

Critical Illness | Complications of Surgical and Medical Care: General Terms | Adverse Reaction to Drug | Sequelae of External Causes of Morbidity and Mortality

Thailand
Universitätsklinikum Hamburg-Eppendorf

Completed

Low-dose Acetylsalicylic Acid Before Non-cardiac Surgery

Surgery | Platelet Dysfunction

Germany
Novartis Pharmaceuticals

Terminated

Myelodysplastic Syndrome (MDS) Gastrointestinal (GI) Tolerability Study (MACS1574)

Myelodysplastic Syndrome | Transfusional Iron Overload

Spain, France, Italy, South Africa
Genelex Corporation
University of Utah

Completed

YouScript IMPACT Registry (IMPACT)

Drug Interaction Potentiation | Adverse Drug Events | Adverse Drug Reactions | Poor Metabolizer Due to Cytochrome P450 CYP2C9 Variant | Drug Metabolism, Poor, CYP2D6-RELATED | Drug Metabolism, Poor, CYP2C19-RELATED | Cytochrome P450 Enzyme Deficiency | Cytochrome P450 CYP2D6 Enzyme Deficiency | Cytochrome... and other conditions

United States
University Hospital, Toulouse

Completed

International Prospective Study on Morphine-induced Adverse Drug Reactions in Emergency Departments. (EI-Morphinique)

Emergencies

France
Boehringer Ingelheim

Completed

Combined Bronchodilators in Chronic Obstructive Pulmonary Disease and the Risk of Adverse Cardio-pulmonary Events

Pulmonary Disease, Chronic Obstructive

Canada
Mahidol University
amfAR, The Foundation for AIDS Research

Unknown

Rilpivirine in Virologically Suppressed Adolescents

HIV
Novartis

Completed

Conversion Trial From Mycophenolate Mofetil (MMF) to Enteric-coated Mycophenolate Sodium (EC-MPS) in Stable Transplanted Patients Suffering From Gastrointestinal (GI) Adverse Events While on Mycophenolate Mofetil Therapy (MMF) Therapy

Liver Transplantation | Kidney Transplantation

Switzerland
General Hospital of Chinese Armed Police Forces

Completed

Different LD of Ticagrelor for Antiplatelet Effect in Patients With Non-ST-segment Elevation ACS Undergoing PCI

Non ST Segment Elevation Acute Coronary Syndrome

China
Hoffmann-La Roche

Completed

An Observational Study on The Prediction of Adverse Events in Patients With Chronic Hepatitis C Receiving a Long-Acting Interferon Plus Ribavirin (GUARD-C)

Hepatitis C, Chronic

Belgium, Greece, Slovakia, Hungary, Italy, Korea, Republic of, Poland, Romania, Bosnia and Herzegovina, Serbia, Brazil, Morocco, Portugal, India, Egypt, Pakistan, Lebanon, Kuwait, Macedonia, The Former Yugoslav Republic of, Qatar and more
Hoffmann-La Roche

Completed

An Observational Study on Infusion-related Adverse Events at Administration of MabThera (Rituximab) in Patients With Chronic Lymphocytic Leukemia

Lymphocytic Leukemia, Chronic

Sweden
Daewoong Pharmaceutical Co. LTD.

Withdrawn

Observational Study to Assess the Incidence Rate of the Major Adverse Cardiovascular Events (MACE) and Safety of Fenofibrate (Lipilfen Capsule)

Metabolic Syndrome

Korea, Republic of
Hospices Civils de Lyon

Completed

Antibiotic-related Serious Adverse Events in Obese Patients Treated for Bone and Joint Infection

Obesity

France
Shanghai Jiao Tong University School of Medicine
Changhai Hospital; Ministry of Science and Technology of the People´s Republic...

Terminated

Shanghai Registry of Acute Coronary Events

Coronary Artery Disease | Acute Coronary Syndrome

China
RWTH Aachen University

Completed

Quality of Telemedically Guided Prehospital Analgesia

Analgesia | Telemedicine | Adverse Events | Prehospital | Ambulance | Opioids | Teleconsultation | Tele-emergency Medical Services | City of Aachen | Prehospital Emergency Medical Service Physician

Germany
Imperial College London
Medical Research Council; Wellcome Trust

Completed

Investigating Immunisation Strategies of DNA, MVA and CN54rgp140 Adjuvanted With GLA-AF to Maximise Antibody Responses (UKHVCSpoke003)

HIV

United Kingdom
F2G Biotech GmbH
Simbec-Orion Group

Completed

Single Ascending Oral Dose Study of F901318

Invasive Aspergillosis

United Kingdom
Lin, Hsi-Hsun, M.D.

Completed

Sustained Virological Suppression and Improvement of Adverse Events of Switching to Raltegravir Study (TaISENWITCH)

HIV Infection | Quality of Life | Adverse Drug Reaction

Taiwan
National Heart, Lung, and Blood Institute (NHLBI)

Withdrawn

Adverse Events With Magnesium Sulfate

Lung Diseases

United States
David Antoniucci
A.R. CARD Onlus Foundation

Terminated

BLeeding Events and Maintenance DoSe of PraSugrel (BLESS)

Acute Coronary Syndrome | Adverse Reaction to Antiplatelet Agent

Italy
Sultan Qaboos University

Completed

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

Adverse Drug Events
The University of Texas Health Science Center,...

Completed

The Effect of Caffeine on Postextubation Adverse Respiratory Events in Children With Obstructive Sleep Apnea (OSA). (OSA)

Sleep Apnea, Obstructive | Postoperative Complications | Tonsillectomy | Adenoidectomy

United States
University of British Columbia
Icahn School of Medicine at Mount Sinai; Vancouver Coastal Health

Unknown

Adverse Events and Genomics in Schizophrenia (AEGIS)

Adverse Effect of Other Antipsychotics and Neuroleptics

Canada
Eduardo Barbosa Coelho

Completed

CYP4A11 and CYP4F2 Gene Variants as Makers of Cardiovascular Adverse Events of Non-steroidal Anti-inflammatory Drugs

Drug-Related Side Effects and Adverse Reactions

Brazil
Elpen Pharmaceutical Co. Inc.

Completed

Antiplatelet Therapy Following Stent Implantation (Anti-Clot)

Angina, Unstable | Acute Myocardial Infarction | Coronary Syndrome

Greece
Puma Biotechnology, Inc.

Completed

Open-label PK Study to Evaluate Lansoprazole and Neratinib in Healthy Subjects

Healthy

United States
Meir Medical Center

Unknown

Assessment of Adverse Cardiac Events Using Local Anesthesia With Adrenaline

Arrythmia
Asan Medical Center

Unknown

Photodynamic Therapy in Locally Advanced Hilar Cholangiocarcinoma (PDT)

Feasibility | Adverse Events | Treatment Response

Korea, Republic of
Sunnybrook Health Sciences Centre

Completed

A Genetic and Perfusion Study of Response to Cognitive Enhancers in Lewy Body Disease

Lewy Body Disease

Canada
Cairo University

Completed

Efficacy of Different Perioperative Statin Regimens on the Protection Against Post Coronary Artery Bypass Grafting Major Adverse Cardio-cerebral Events

Coronary Artery Bypass Grafting
Fundación Andaluza de Reumatología

Completed

Study to Assess the Management of Synthetic Disease-modifying Antirheumatic Drug (DMARD) at the Onset of Adverse Events, Intolerance or Lack of Efficacy in Rheumatoid Arthritis (RA) (SAR-FAME)

Rheumatoid Arthritis

Spain
AstraZeneca

Completed

Observational Prospective Study OPTIMA II - Follow-up (OPTIMAII)

Major Adverse Cardiovascular and Cerebrovascular Events (MACCE)

Russian Federation
Singapore Clinical Research Institute
Singapore General Hospital; Duke-NUS Graduate Medical School

Terminated

The Effect of 90-day Oral Testosterone Therapy in Chinese Males With Type 2 Diabetes (T2DM) (OTEST)

Assess the Effects of a the 90-day Oral TS Study Regimen on PSA, IPSS, Haemoglobin and Haematocrit, and to Assess Adverse and Serious Adverse Events.

Singapore
University of Pittsburgh
RAND

Completed

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

Adverse Drug Events

United States

Search clinical trials for: Adverse drug events

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