Questions to Ask Before Participating In a Clinical Research Trial! - PowerPoint PPT Presentation

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Questions to Ask Before Participating In a Clinical Research Trial!

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Want to become a part of clinical research? Then Vial Trials is the right spot for you. To know questions to ask before participating in a clinical research trial, read this blog here! – PowerPoint PPT presentation

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Title: Questions to Ask Before Participating In a Clinical Research Trial!


1
Questions to Ask Before Participating In a
Clinical Research Trial!
2
  • If you take part in a clinical trial, you may get
    tests or treatments in a hospital, clinic, or
    doctors office. Participants in a clinical
    trial are often treated like other patients who
    arent in a clinical trial but are more
    carefully monitored and may have more tests done.
  • Clinical trials take place in doctors offices,
    medical centers, community hospitals and
    clinics, and veterans hospitals worldwide. A
    particular trial may be offered at only one
    location, but some are conducted at many
    different hospitals worldwide. From  clinical
    research patient recruitment  to study
    completion, Principal Investigators (PI) must
    undertake many tasks.

3
What Types Of Trials Are?
  • Before participating in a clinical trial, it is
    necessary to consider which types of the trail
    are participating. According to the National
    Institutes of Health, there are at least six
    different types of clinical trials. It includes
  • Prevention
  • Screening
  • Diagnostic
  • Treatment
  • Behavioral
  • Quality
  • Each clinical trial involves different degrees of
    risk. Yes, like screening, diagnostic, and
    treatment trials may carry varying degrees of
    higher risk, while prevention, behavioral and
    quality clinical trials are present low risk. So,
    consider all these things carefully. 

4
How Are Clinical Trials Designed?
  • When professionals conduct a clinical trial,
    clinical research organizations (like us) must
    design clinical trials. Yes, it is necessary
    because these designs ensure that each trial is
    valuable, needed, and safe.

5
What about Informed Consent?
  • The purpose of the informed consent process is to
    ensure that the patient fully understands all of
    the information and implications of the clinical
    trial. Patients can ask as many questions as they
    want and for clarification of points already
    discussed. In addition, if a patient agrees to
    undergo a clinical trial and then changes
    their mind, they may withdraw at any time.

6
What Factor Should You Consider When Deciding To
Participate In A Clinical Trial?
  • Factors that allow someone to participate in a
    therapeutic areas clinical research are
    inclusion criteria. Those that exclude or do
    not allow participation are exclusion
    criteria. These criteria are based on age,
    gender, the type and stage of a disease,
    previous treatment history, and other medical
    conditions.

7
Some other questions that you should ask
  • What is the study medication expected to help
    with?
  • How long will the trial last?
  • What are the risks?
  • What are the possible risks and benefits, and
    options if I am harmed?
  • What kinds of treatment, procedures, or
    tests will I undergo during the trial?
  • What are the side effects of the tests or
    treatments?
  • Will I be able to take my regular medications
    while participating

8
  • Participating in a clinical trial is a serious
    decision that should not be entered into lightly.
    For your health concern, talking to your doctor
    or another trusted healthcare provider is very
    necessary. They will help you understand a
    possible trial.

9
Thank You
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