Available Clinical Trial Studies
Study Area of Interest*
Location*
Study Area of Interest*
Location*
Available Clinical Trial Studies
Study Area of Interest*
Location*
Study Area of Interest*
Location*
- CenExel Atlanta, GA
- 501 Fairburn Road SW
Abdominoplasty
An abdominoplasty, also called a tummy tuck, is a surgery to make the belly look flatter. During the surgery, doctors remove extra skin and fat from the stomach area. They may also tighten the muscles underneath the skin. This can help the tummy look smoother and feel firmer.
- CenExel Atlanta, GA
- 501 Fairburn Road SW
- Age 18+
- Male, Female
- Enrolling
- CenExel Atlanta, GA
- 501 Fairburn Road SW
Alzheimer’s Disease
Alzheimers disease is the most common type of dementia. It often starts with mild memory loss but can progress to serious problems, such as difficulty having conversations or responding to surroundings. The disease affects parts of the brain responsible for memory, thinking, and language, making it hard to do everyday tasks.
- CenExel Atlanta, GA
- 501 Fairburn Road SW
- Age 55
- -85
- Male, Female
- Upcoming
- CenExel Los Alamitos, CA
- 3771 Katella Ave, #300
Alzheimer’s Disease
Alzheimer’s disease is the leading cause of dementia and typically begins with mild memory impairment. As the disease advances, it can cause significant challenges, such as trouble communicating or reacting to the environment. Alzheimer’s impacts areas of the brain responsible for memory, thought processes, and language, making daily activities increasingly difficult.
- CenExel Los Alamitos, CA
- 3771 Katella Ave, #300
- Age 50
- -80
- Male, Female
- Enrolling
- CenExel Marlton, NJ
- 401 Route 73 N | 30 Lake Center Executive Park, #100
Alzheimer’s Disease
Alzheimers disease is the most common type of dementia. It starts with mild memory loss and can lead to more serious problems, like not being able to talk or respond to the world around you. Alzheimers affects parts of the brain that control thinking, memory, and language, making it hard for people to do everyday tasks.
- CenExel Marlton, NJ
- 401 Route 73 N | 30 Lake Center Executive Park, #100
- Age 55
- -85
- Male, Female
- Enrolling
State-of-the-art Facilities
Our award-winning Centers are held to the highest quality standards in medical equipment technology, cleanliness, and comfort.
Board-certified Physicians
Our medical staff and professional researchers are seasoned experts in their areas of expertise and the clinical trial field.
Safe, Approved Procedures
Clinical research methods undergo rigorous evaluation and scrutiny, similar to the standards at any other hospital or clinic.
Register today to see if you qualify.
Frequently Asked Questions
What is a CenExel Center of Excellence?
CenExel Centers of Excellence are leaders in the clinical trial world, improving lives through new and better medicines. Our Centers prioritize quality of care and participant safety. Our Principal Investigator physicians are board-certified medical research experts, and our professional support staff is highly experienced as well. We regularly revisit training and best practices to ensure first-class care. CenExel state-of-the-art facilities are spacious, comfortable, and appropriately private.
How do clinical trials work?
While the clinical study process varies for each trial, there are certain steps that regularly occur. Before you begin a study, all procedures and details will be thoroughly explained to you. Over the course of the study, the Study Coordinator and Principal Investigator physician will assist you and answer questions. They will check your health at the beginning of the trial, give you specific instructions for participating, monitor you carefully during the trial, and stay in touch with you after the study.
Some clinical trials involve more tests and doctor visits than you would normally have for your illness or condition. Your participation will be most successful if you carefully follow all instructions you are given and stay in contact with the research staff.
How safe are clinical studies?
There are many safeguards in place that all research organizations must follow when conducting clinical trials. At CenExel, we proudly adhere to these safeguards and take additional steps to ensure participant safety and comfort.
The Food and Drug Administration (FDA) is the regulatory agency that oversees all clinical research conducted in the United States. It is their responsibility to protect the rights and, as much as possible, the welfare of subjects participating in clinical trials. The FDA reviews the data collected from clinical trials because they ultimately determine whether a new treatment should be sold in the U.S. Several organizations and individuals are governed by FDA regulations including clinical investigators, pharmaceutical sponsors (the companies developing the treatments), Contract Research Organizations (companies that help conduct the studies), and Institutional Review Boards (groups that are responsible for ensuring the safety and welfare of study participants).
Good Clinical Practice (GCP) guidelines are industry guidelines designed to protect the safety of trial subjects. These guidelines encompass federal regulations and industry-accepted standards that govern clinical trials. These regulations and standards apply to the conduct of the studies, record keeping, informed consent of subjects, collection of scientific data, and submission of information needed for the FDA to determine whether a new treatment should be sold in the U.S. All research organizations must follow these guidelines when conducting clinical research.
An Institutional Review Board (IRB) is a committee that is formally tasked by an institution to review, approve, and monitor research involving human subjects. IRBs ensure that the risks to subjects are minimized; that subjects are adequately informed about the trial and the implications it will have on their treatment; that study protocols are modified, when necessary, to ensure safety; that risks are reasonable in relation to the anticipated benefits and the importance of the knowledge to be gained; that subject selection is equitable and that no classes of patients are discriminated against; that informed consent is obtained; that there is a provision for safety monitoring in the research plan; and that there are adequate provisions for the privacy and confidentiality for subjects and the data collected.