Adverse Reaction Clinical Trials

2 recruiting

Adverse Reaction Trials at a Glance

55 actively recruiting trials for adverse reaction are listed on ClinicalTrialsFinder across 6 cities in 32 countries. The largest study group is Not Applicable with 17 trials, with the heaviest enrollment activity in Madrid, Xining, and Barcelona. Lead sponsors running adverse reaction studies include Jiuda Zhao, Mahidol University, and Masaryk University.

Browse adverse reaction trials by phase

Treatments under study

About Adverse Reaction Clinical Trials

Looking for clinical trials for Adverse Reaction? There are currently 2 studies actively recruiting participants. Clinical trials offer access to new treatments before they are widely available, and every approved therapy in use today was first tested through a clinical trial.

Below you can browse trials, sign up for alerts when new Adverse Reaction trials open, and view eligibility criteria for each study. Each listing includes the study phase, locations, and enrollment details.

Frequently Asked Questions

Common questions about Adverse Reaction clinical trials

A clinical trial is a carefully designed research study that tests new medical treatments, drugs, devices, or approaches in human volunteers. Every approved medication and treatment available today was proven safe and effective through clinical trials.

All clinical trials are reviewed and approved by Institutional Review Boards (IRBs) — independent committees that evaluate patient safety. Trials follow strict protocols, and your health is monitored closely throughout. You can withdraw at any time.

Not necessarily. Many trials compare the new treatment against the current standard of care, meaning all participants receive active treatment. When placebos are used, they are typically combined with standard treatment, not given alone. The trial description will always specify the design.

Under the Affordable Care Act, most private insurers are required to cover routine patient care costs during a clinical trial. The sponsor typically covers the investigational treatment itself. Medicare also covers routine costs for qualifying trials.

Yes. Participation is completely voluntary. You can withdraw at any time, for any reason, without it affecting your access to standard medical care.

Each trial has specific eligibility criteria — including age, diagnosis, disease stage, prior treatments, and general health. Browse the trials listed above and check their eligibility sections. You can also contact the trial site directly to discuss your situation.

Showing 120 of 55 trials

Recruiting
Not Applicable

COOLEY- Study: aCute On chrOnic Liver failurE Using the cYtosorb Device

SarcopeniaUltrasonographyAcute-On-Chronic Liver Failure+1 more
University Hospital, Antwerp20 enrolled1 locationNCT06079021
Recruiting

Genomics and COVID-19 Vaccine Adverse Events

Vaccine Adverse Reaction
University of British Columbia6,325 enrolled1 locationNCT05212792
Recruiting

IMMUNO-FIT Observational Study

Quality of LifeNeoplasmsImmunotherapy+2 more
University Hospital Southampton NHS Foundation Trust67 enrolled1 locationNCT07354971
Recruiting
Phase 2

A Study to Evaluate LY3537021 for the Treatment of Nausea and Vomiting Caused by Chemotherapy in Adults With Cancer

NeoplasmsVomitingNausea+1 more
Eli Lilly and Company204 enrolled66 locationsNCT07169851
Recruiting
Phase 4

Antihistamine for Prevention of HTR After Blood Primed CPB

Blood Transfusion Associated Adverse Reactions
Kasr El Aini Hospital40 enrolled1 locationNCT07536152
Recruiting
Not Applicable

Telenursing for the Early Detection and Management of Side Effects Associated With Cyclin-Dependent Kinase Inhibitors in Breast Cancer Patients

Breast CancerDrug-Related Side Effects and Adverse Reactions
Azienda Sanitaria Locale di Asti124 enrolled1 locationNCT07524829
Recruiting
Phase 1

Safety and Efficacy of LOw DOse COlchicine in Patients With STatin INTolerance: the LODOCO STINT Pilot Study

Statin Adverse Reaction
Virginia Commonwealth University30 enrolled1 locationNCT06874192
Recruiting
Not Applicable

Stop or Ongoing Oral Anticoagulation in Patients Undergoing Pvp (SOAP)

Benign Prostatic HyperplasiaAnticoagulant Adverse Reaction
Clinique Pasteur389 enrolled1 locationNCT03297281
Recruiting

Blood Storage Related Mortality and Adverse Effects in Trauma Patients

Transfusion Adverse Reaction
Kocaeli City Hospital300 enrolled1 locationNCT07341139
Recruiting
Not Applicable

Comparison of Cough Response Between Tegilidine and Sufentanil as Pre-induction Agents in General Anesthesia

General Anesthetic Drug Adverse Reaction
The First People's Hospital of Lianyungang190 enrolled1 locationNCT07323043
Recruiting
Phase 3

Propofol and Etomidate Admixtures Comparisons Trial (PEAC Trial)

AnesthesiaAnesthesia ComplicationAnesthesia; Reaction+3 more
University of Texas Southwestern Medical Center200 enrolled1 locationNCT05358535
Recruiting

Optimization of Perioperative Antibiotic Prophylaxis in Patients Allergic to Beta-lactams in the Orthopedic Surgery and Trauma Departments

Beta Lactam Adverse Reaction
University Hospital, Strasbourg, France50 enrolled1 locationNCT07342647
Recruiting
Not Applicable

Exercise Therapy for Isotretinoin Users

IsotretinoinIsotretinoin Adverse Reaction
Uşak University160 enrolled1 locationNCT07196787
Recruiting
Phase 2

Oral Glibenclamide in Preterm Infants With Hyperglycaemia (GALOP)

PretermTransient; Hypoglycemia, NeonatalGlibenclamide Adverse Reaction
Assistance Publique - Hôpitaux de Paris35 enrolled1 locationNCT05687500
Recruiting

Anticholinergic Burden and Osteoporosis in Rheumatoid Arthritis

Fractures, BoneRheumatoid Arthritis (RA)Anticholinergic Adverse Reaction
Balikesir University100 enrolled1 locationNCT06812481
Recruiting
Not Applicable

Effects of Flumazenil on Recovery After Total Intravenous Anesthesia With Remimazolam

Elderly PatientsRemimazolamFlumazenil Adverse Reaction+1 more
Pusan National University Yangsan Hospital24 enrolled1 locationNCT05939674
Recruiting
Not Applicable

Comparative Study of Tranexamic Acid Dosing in Cardiac Surgery

Adverse Drug EventFibrinolysis; HemorrhageBlood Coagulation Disorder+2 more
University of Ioannina150 enrolled1 locationNCT07164300
Recruiting

Ultrasound Evaluation of Hematoma Risk After Needle EMG in Patient on DOAC Therapy

Neuromuscular Diseases (NMD)PolyneuropathiesPeripheral Neuropathies+4 more
Masaryk University70 enrolled2 locationsNCT07166302
Recruiting

Pharmacogenomics of Selective Serotonin Reuptake Inhibitor (SSRI)-Induced Behavioural Activation

Behavioral ActivationMajor Depressive DisorderAnxiety Disorders+3 more
University of Manitoba160 enrolled2 locationsNCT06763081
Recruiting
Phase 4

Effect of Mannitol on Propofol Level

Mannitol Adverse Reaction
Cukurova University40 enrolled1 locationNCT06884657