Understanding HIV-Related Clinical Trials
Table of Contents
The term clinical trial is used to describe many different types of research studies. There are five main types of clinical trials:
The scientists and health care providers who manage clinical trials are usually called investigators. The people who join clinical trials are usually called participants, but may be referred to as volunteers or study subjects. ALL clinical trials are voluntary -- you never have to participate in a clinical trial unless you want to.
Each clinical trial has a written plan, or study protocol, that describes the goals of the study, how long the study will last, which people are eligible to participate (also called inclusion and exclusion criteria), and what tests and procedures are required of each participant.
Inclusion and exclusion criteria are the guidelines used to determine who can and cannot participate in a specific clinical trial. Inclusion criteria are requirements that a person must meet to participate (such as CD4 cell count, viral load, or age). Exclusion criteria are factors that prevent a person from participating either for his or her safety or to make it easier to understand the study results. For example, people might be excluded for having liver problems, or if they have already used a drug that is being studied.
Each participant in a clinical trial must sign an informed consent. When you sign this document it means that you understand the details of the study and you agree to participate. You may also want to take the document with you and talk about the study with your health care provider, family, or friends before you decide to participate. If your native language is not the language spoken by the people describing the study, you may ask if translation is available. It is important that you truly understand the study and what you will be asked to do. If you have any questions, be sure to ask the study staff. It is their job to make sure that, when you sign, you are making an informed choice.
You may be paid for travel expenses to and from the study site and for your time. Childcare may also be provided. You can choose to drop out of a study at any point and for any reason.
The most common type of clinical trial in HIV is a treatment or drug study. There are four stages, or phases, of clinical trials for new treatments. With each phase, a little more is known about the treatment being studied. Each phase has a different purpose and helps researchers answer specific questions about the drug in trial.
Once a drug trial has completed the first three phases of research, the company that makes the drug submits the study data to the FDA for approval. Because the need for treatments for HIV is so great, a drug company can apply for something called accelerated approval if its drug offers something new or meets a need for people living with HIV (HIV+).
Accelerated approval happens faster than regular drug approval and it may put special restrictions on how the drug can be used. However, even if a drug gets accelerated approval, the drug company must continue doing long-term research on the drug for it to get full approval.
This article was provided by The Well Project. Visit The Well Project's Web site to learn more about their resources and initiatives for women living with HIV. The Well Project shares its content with TheBody.com to ensure all people have access to the highest quality treatment information available. The Well Project receives no advertising revenue from TheBody.com or the advertisers on this site. No advertiser on this site has any editorial input into The Well Project's content.
Add Your Comment:
Internet search results. Be careful when providing personal information! Before
adding your comment, please read TheBody.com's Comment Policy.)