- Health Outcomes
- Health Outcomes measures the impact (what happens) to an individual who has received a certain treatment (could be an experimental drug, diet, exercise, etc.) Health Outcomes can include a wide range of measures, such as medical tests, frequency of doctor's visits, frequency of emergency room visits, patient satisfaction, patient preferences, and health related quality of life.
- Immune system
- Your bodyÕs defense system against infection and certain diseases.
- In Vitro Testing
- Laboratory testing that does not involve animals or humans.
- In Vivo Testing
- Testing in animal and humans.
- The number of new cases of infection or disease occurring in a specific population in a given time period.
- Inclusion and Exclusion Criteria
- The rules that determine whether or not someone is eligible to enter a clinical trial. These rules are based on such factors as age, gender, the type and stage of a disease, previous treatment history, and other medical conditions.
- Informed Consent
Informed consent means deciding if you want to take part in
This decision is only made after:
1. A study staff person has explained the study
2. You understand the purpose of the study, and
3. You really understand what you will have to do while in the study.
A person responsible for the conduct of the clinical trial
at a trial site. If a trial is conducted by a team of
individuals at a trial site, the investigator is the
responsible leader of the team and may be called the
Investigators are listed on the GSK CSR only for those study sites that proceed to enrol research subjects in to the study protocol. Investigators are not listed if the site does not enrol subjects – for example if the overall study completes before the individual site is able to begin recruitment.