Advertisement
MDchoice.com
We subscribe to the HONcode principles
of the Health On the Net Foundation


Health Information
Friday, September 05, 2008
Find more information about this topic from either the Web or the world's best medical journals by using the search boxes at the top of this page.
 


Glossary A - H

Action studies: In cancer prevention clinical trials, studies that focus on finding out whether actions people take can prevent cancer.

Agent studies: In cancer prevention clinical trials, studies that focus on examining whether taking certain medicines, vitamins, minerals, or food supplements can prevent cancer.

Benign: Not cancerous; cannot invade neighboring tissues or spread to other parts of the body.

Bias: Having an idea about what the study results will show before the clinical trial is conducted.

Chemoprevention studies: Also called "cancer prevention agent studies." Cancer prevention studies that test whether the study agent  usually medicines, vitamins, minerals, food supplements, or a combination of them  can reduce a person's chances of getting cancer.

Clinical trials: Also called "clinical studies." Research studies with people. Each trial tries to answer specific scientific questions and to find better ways to prevent, detect, or treat diseases or to improve care.

Colon polyps: Abnormal growths of tissue on the lining of the bowel. Polyps are a risk factor for cancer of the bowel.

Consent form: A document that provides key facts about a clinical trial. This includes information about the study agent, tests that study participants may have, and possible benefits and risks. Although all participants in a clinical trial must sign a consent form, they can leave the study at any time. As a trial proceeds, there may be new consent forms.

Control group: In a Phase III cancer prevention clinical trial of a study agent, the group that receives either a placebo or a standard agent that is being compared to a new agent.

Data Safety and Monitoring Committee: An impartial group that provides oversight of a clinical trial and reviews the results to see if they are acceptable. This group determines if the trial should be altered or closed.

Double-blind: A method used to prevent bias in a clinical trial. Neither the participants nor the doctor knows who is taking the study agent and who is not. Only researchers at a central office know.

Environmental risk factor: A hazardous agent that is known to cause cancer or increase risk when people are exposed to it, for example asbestos, radon, and second-hand smoke.

Followup: Keeping track of the health of people who participate in a clinical study for a period of time during the study and after the study ends.

Gene alterations: Changes in the cells' unit of inheritance that may be good or bad for the body.

Hereditary risk factor: Altered or mutated genes that make it more likely that a person will develop cancer. Also called an "inherited" risk factor, but this does not necessarily have to be inherited from a parent. It can be acquired in a germline cell through lifestyle behaviors or through exposure to hazards in the environment. Once this cell is altered, the mutated gene can pass to the next generation.



Back


National Cancer Institute
April 1999