Clinical Study Process

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Discover our study guide for a clear understanding of the process and how easy it is to participate.

Clinical Study Process

Let us show you how it happens.

Pre-
screening

Potential participants undergo initial screening to determine if they meet the study’s eligibility criteria.

Informed consent

Participants receive information about the study and must provide written consent to participate.

Baseline assessment

Participants undergo a baseline assessment to establish their health status and to establish a baseline for comparison with later assessments.

Randomization

Participants are randomly assigned to either the treatment group or the control group.

Treatment

Participants in the treatment group receive the study intervention, while those in the control group receive a placebo or standard treatment.

Dissemination

Study results are disseminated through publications and presentations to the medical community and the public.

Data analysis

Potential participants undergo initial screening to determine if they meet the study’s eligibility criteria.

Endpoint assessment

Participants undergo a final assessment to determine the study endpoint, which may be a clinical outcome or a laboratory measurement.

Adherence monitoring

Participants are monitored for adherence to the study protocol and treatment regimen.

Follow-up

Participants are regularly assessed to monitor their response to the intervention and to detect any adverse effects.

FREQUENTLY ASKED QUESTIONS

Want to learn more about Analytica Medical Studies? Have a question about our process? The answers to these and more can be found in our FAQ page!

Analytica Medical

Decentralized clinical studies enabling health science champions nationwide.