Explore Diagnostic Clinical Trials. Your participation is not only welcomed but also vital in advancing and improving diagnostic testing methods.
Blood Test for Alzheimer's
This paid clinical trial in Morton, IL, evaluates the effectiveness of a new Alzheimer’s biomarker blood test. Healthy volunteers will participate in a brief cognitive assessment, followed by a blood draw. By closely examining these samples, the study aims to advance our understanding of Alzheimer’s disease and enhance early detection efforts. The findings from this research will play a crucial role in preventing the onset of Alzheimer’s and promoting long-term brain health.
Eligibility Criteria
Age
55 and older
Gender
Male & Female
Condition
No memory concerns
Location
Morton, IL
Status
Recruiting
COVID-19, Flu, and RSV Diagnostic Clinical Trials: Quick, Simple, and Safe
At Clinical Research, our diagnostic clinical trials for COVID-19, flu, and RSV are designed to be fast, easy, and non-invasive. Each study typically involves just two quick nasal swabs, with the entire process taking about 30 minutes.
These tests are safe and reliable, following strict guidelines from the U.S. Food and Drug Administration (FDA). While no test is 100% accurate, especially with evolving viruses, the FDA ensures that all diagnostic tests meet rigorous safety and accuracy standards before they are made available to the public. This helps ensure that the results you receive are dependable, offering valuable insights for diagnosing respiratory infections.
Eligibility Criteria
Age
2+
Gender
Male & Female
Condition
Nasal swab tests
Location
Morton, IL
Status
Recruiting
Enrollment Process
Clinical trials are essential for advancing medical knowledge and improving patient care by testing the efficacy and safety of potential treatments before they are widely available to the public. Here’s what you can expect when considering enrollment.
Recruitment
Recruiting volunteers is the first step of an active clinical trial.
Phone Screening
You will undergo a phone screening to determine your eligibility.
Informed Consent
You must sign an ICF defining the purpose, procedure, potential risks & benefits, and your rights as participants.
