Clinical study design

Source: Wikipedia, the free encyclopedia.

Clinical study design is the formulation of trials and experiments, as well as observational studies in medical, clinical and other types of research (e.g., epidemiological) involving human beings.[1] The goal of a clinical study is to assess the safety, efficacy, and / or the mechanism of action of an investigational medicinal product (IMP)[2] or procedure, or new drug or device that is in development, but potentially not yet approved by a health authority (e.g. Food and Drug Administration).[3] It can also be to investigate a drug, device or procedure that has already been approved but is still in need of further investigation, typically with respect to long-term effects or cost-effectiveness.[4]

Some of the considerations here are shared under the more general topic of design of experiments but there can be others, in particular related to patient confidentiality and ethics.

Outline of types of designs for clinical studies

Treatment studies

Observational studies

1. Descriptive

2. Analytical

Important considerations

When choosing a study design, many factors must be taken into account. Different types of studies are subject to different types of bias. For example, recall bias is likely to occur in cross-sectional or case-control studies where subjects are asked to recall exposure to risk factors. Subjects with the relevant condition (e.g. breast cancer) may be more likely to recall the relevant exposures that they had undergone (e.g. hormone replacement therapy) than subjects who don't have the condition.[citation needed]

The ecological fallacy may occur when conclusions about individuals are drawn from analyses conducted on grouped data. The nature of this type of analysis tends to overestimate the degree of association between variables.[citation needed]

Seasonal studies

Conducting studies in seasonal indications (such as allergies,

Seasonal Affective Disorder, influenza, and others) can complicate a trial as patients must be enrolled quickly. Additionally, seasonal variations and weather patterns can affect a seasonal study.[15][16]

Other terms

See also

References

  1. .
  2. ^ "Investigational Medicinal Product (IMP) | Noclor". www.noclor.nhs.uk. Archived from the original on 2020-09-26. Retrieved 2019-11-19.
  3. ^ Ann (April 14, 2006). "Clinical Study Management". ProMedica International. Retrieved June 4, 2019.
  4. ^ Nichols, Hannah (May 18, 2018). "How do clinical trials work and who can participate?". Medical News Today. Retrieved June 4, 2019.
  5. ^ Shiel, William C. Jr. (December 21, 2018). "Randomized control trial". Medicine Net. Retrieved June 4, 2019.
  6. ^ "Are these data real? Statistical methods for the detection of data fabrication in clinical trials". The BMJ. July 28, 2005. Retrieved June 4, 2019.
  7. ^ Shiel, William C. Jr. (December 21, 2018). "Nonblinded study". Medicine Net. Retrieved June 4, 2019.
  8. PMID 20927243
    .
  9. ^ "NCI Dictionary of Cancer Terms". National Cancer Institute. 2 February 2011. Retrieved June 4, 2019.
  10. PMID 26058820
    .
  11. ^ .
  12. ^ "NCI Dictionary of Cancer Terms". National Cancer Institute. 2 February 2011. Retrieved June 4, 2019.
  13. ^ "NCI Dictionary of Cancer Terms". National Cancer Institute. 2 February 2011. Retrieved June 4, 2019.
  14. ^ "NCI Dictionary of Cancer Terms". National Cancer Institute. 2 February 2011. Retrieved June 4, 2019.
  15. ^ Yamin Khan; Sarah Tilly. "Flu, Season, Diseases Affect Trials". Applied Clinical Trials Online. Archived from the original on 11 July 2011. Retrieved 26 February 2010.
  16. ^ Yamin Khan; Sarah Tilly. "Seasonality: The Clinical Trial Manager's Logistical Challenge" (PDF). published by: Pharm-Olam International (POI). Archived from the original (PDF) on 15 July 2011. Retrieved 26 April 2010.
  17. ^ "Prospective vs. Retrospective Studies". Stats Direct. Retrieved May 30, 2019.

External links