Dr. Craig Heigerick - Principal Investigator

Dr. Craig Heigerick - Principal Investigator

Dr. Craig Heigerick - Principal Investigator

Dr. Craig Heigerick - Principal Investigator

Dr. Craig Heigerick - Principal Investigator

Dr. Craig Heigerick - Principal Investigator

Medical Research Atlanta

GCH Research Associates

We Have the Answers to your most Common Questions.

We consider it a privilege to work with you to address your questions and concerns.

What is a clinical research study?

What happens during a clinical study?

What are the benefits of participating in a clinical study?

How am I protected during the research clinical study?

Who participates in clinical research and how are they selected?

Why can't I know which drug I am on?


We consider it a privilege to work with you to address your questions and concerns.

Below are the answers to some of our most frequently asked questions. We would like to help educate you about how clinical trials are conducted and what you can expect from your experience. We want you to have the necessary knowledge to make the best decision for you. After all, it's your choice.

What is a clinical research study?

A clinical research study is a scientific investigation (trial or study) of a research medication or treatment to find out how it works in people. Through clinical studies, doctors help find possible new ways to prevent, detect, diagnose, control and treat illnesses. Before a new medication can be approved for use by the public, it must be tested thoroughly according to strict guidelines established by the U.S. Food and Drug Administration (FDA). Participation in clinical studies is completely voluntary and all information provided by a participant is kept strictly confidential and used only for the purposes of conducting the study as required by law.

What happens during a clinical study?

Participation in a clinical study means you will work with a research team in a clinical office setting. Team members include doctors, nurses, study coordinators, and other health care professionals. As a qualified volunteer for a study you will receive all medical visits related to the study at no cost. This can include: physical exams, doctor visits, study medications, laboratory tests, EKG's, etc.

What are the benefits of participating in a clinical study?

Most of our current information on medicines and diseases has been obtained from research. New drugs are being developed daily and may offer advantages over existing ones. Still, being involved in a research study sometimes makes us uneasy. It helps if we remember the many research successes over the past few decades. For example, vaccines and antibiotics have been developed to eradicate many previously common and deadly diseases such as smallpox, polio, diphtheria, tetanus, and childhood leukemia. Some of the many benefits of participating include:

  • Study-related care provided by qualified physicians.
  • Learning more about your illness and the latest available treatments.
  • Receiving study visits and study medication at no cost.
  • Gain access to new drugs and interventions prior to public availability.
  • Provide a valuable contribution to the healthcare industry.
  • Could be contributing to important research that may help you, your grandchildren and future generations.

How am I protected during the research clinical study?

Patient safety is the number one priority of the FDA, the pharmaceutical companies, and GCH Research Associates. Before participating in a study, you will be asked to read and sign an Informed Consent, which gives detailed information about the study, procedures, and medications including the risks. Experienced physicians who have been thoroughly trained and designated as Principal Investigators monitor you throughout the study. As with any medication, there may be unknown risks from participating in the study. An Institutional Review Board (IRB) must review and approve all studies before you are asked to participate in the study. The IRB is made up of scientific and non-scientific members, clergy, administrators, and members of the public. IRB approval of all research is required by U.S. Food and Drug Administration (FDA) to ensure protection of the rights and welfare of patients who are enrolled in clinical trials.

Remember that participating in a clinical study is completely voluntary and you can leave the study at any time if you change your mind.

Who participates in clinical research and how are they selected?

Lots of different people like you and I participate in clinical research. Every study identifies some specific characteristics that the participants should have in order to participate. These characteristics are called eligibility criteria. Some of these characteristics are things like age, general health, a diagnosis of a particular disease, certain symptoms, etc.

Why can't I know which drug I am on?

A key element in any research trials is to have accurate results. The study may either compare a research drug to standard therapy or a placebo (an inactive substance). The study coordinator, physician and you may have no idea whether you are receiving the actual drug or a placebo. This ensures that the study trial has been unbiased in the results and will show how the new medication does or does not work.

Current Studies

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