Clinical Research Locators
Voluntary participation in
clinical medical trials can be a means of obtaining quality
medical care for individuals who do not have health insurance
or other means of affording doctors’ visits and medications.
Clinical trials are conducted
to test newly developed drugs and medical devices to determine
their safety and effectiveness before they are approved for
general recommended use by the public. Research subjects are the
voluntary participants on whom the new medications or devices
are tested. Healthcare professionals,
usually doctors, administering the research drugs or devices
according to the clinical trial guidelines or protocol are
known as principal investigators.
In the
United States, clinical trials must be approved by independent
ethics committees known as institutional review boards (IRBs)
which monitor and review the research activity to protect the
safety and welfare of research subjects. These committees
usually function at the local level and are empowered by the
Food and Drug Administration (FDA) and Department of Health and
Human Services regulations to approve and/or require
modifications of a planned trial protocol prior to approval of
the research or disapprove the research. The monitory role of
the IRB involves conducting regular meetings of its members and
conveying appropriate and important information of a
scientific, regulatory or ethical nature to the principal
investigators involved in the respective clinical trial
throughout the duration of the research activity.
To find
clinical trials for varying conditions and research sites in
various geographic locations visit the following
websites.
- CenterWatch
CenterWatch has one of the larges and most comprehensive global listings of industry-sponsored- and government-sponsored clinical trials on the Internet.
- ClinicalTrials.gov
ClinicalTrials.gov provides patients, family members, and members of the public easy and free access to information on clinical studies for a wide range of diseases and conditions.
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