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GROUP 1 (32-1A)
Bhoopesh kumar garg
Mohit kumar sharma
Om Prakash saini
INFORMED
CONSENT OF THE
PATIENT.
INFORMED
CONSENT OF THE
CLINICAL TRIAL
PARTICIPANT.
• Informed consent (IS) is the process of a
patient's voluntary confirmation of his consent
to participate in a particular study after he has
been familiar with all aspects of the study .
ALL THAT IS NEEDED FOR INFORMED
CONSENT
Patients should know
• About the results of the survey;
• On the presence of the disease, its diagnosis and prognosis;
• About the methods of treatment;
• The risk of various treatments;
• Possible options for medical intervention;
• About their possible positive and negative consequences.
WHO DID/DID NOT OBTAINED INFORMED
CONSENT
• Dr. johnson and dr. Hirsch obtained informed consent.
• Dr. Band did not obtained informed consenT.
ETHICAL PRINCIPLES
FOLLOWED
WHY INFORMED CONSENT IS NECESSARY?
• To protect rights of both patient and doctor.
• Create awareness
• Create trust between patient and doctor
• Reduces risk of any legal action.
THE INFORMED CONSENT
CONTAINS
• Complete details
• Full acknowledgemenT
HOW WOULD YOU DO IT
DIFFERENTLY?
• Proper procedure
• No hurries in any procedure
HOW WOULD YOU DO IT
DIFFERENTLY?
• The document will contain seven points:
• Introduction.
• Why is there a study?
• Are there any dangers that threaten me?
• What are the benefits of doing research?
• How will the research be conducted?
• What will be required of me, and will I be limited in anything?
• Confidentiality guarantees.
• https://www.ncbi.nlm.nih.gov/books/NBK430827/
• https://www.ncbi.nlm.nih.gov/books/NBK538279/
• https://www.healthline.com/health/informed-consent
• https://en.wikipedia.org/wiki/Informed_consent
• https://www.sciencedirect.com/

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Done by Sharma mohit kumar , garg Bhoopesh kumar, om praksh saini week 6.pptx

  • 1. Submitted by GROUP 1 (32-1A) Bhoopesh kumar garg Mohit kumar sharma Om Prakash saini
  • 2. INFORMED CONSENT OF THE PATIENT. INFORMED CONSENT OF THE CLINICAL TRIAL PARTICIPANT.
  • 3. • Informed consent (IS) is the process of a patient's voluntary confirmation of his consent to participate in a particular study after he has been familiar with all aspects of the study .
  • 4. ALL THAT IS NEEDED FOR INFORMED CONSENT
  • 5. Patients should know • About the results of the survey; • On the presence of the disease, its diagnosis and prognosis; • About the methods of treatment; • The risk of various treatments; • Possible options for medical intervention; • About their possible positive and negative consequences.
  • 6. WHO DID/DID NOT OBTAINED INFORMED CONSENT • Dr. johnson and dr. Hirsch obtained informed consent. • Dr. Band did not obtained informed consenT.
  • 8. WHY INFORMED CONSENT IS NECESSARY? • To protect rights of both patient and doctor. • Create awareness • Create trust between patient and doctor • Reduces risk of any legal action.
  • 9. THE INFORMED CONSENT CONTAINS • Complete details • Full acknowledgemenT
  • 10. HOW WOULD YOU DO IT DIFFERENTLY? • Proper procedure • No hurries in any procedure
  • 11. HOW WOULD YOU DO IT DIFFERENTLY? • The document will contain seven points: • Introduction. • Why is there a study? • Are there any dangers that threaten me? • What are the benefits of doing research? • How will the research be conducted? • What will be required of me, and will I be limited in anything? • Confidentiality guarantees.
  • 12. • https://www.ncbi.nlm.nih.gov/books/NBK430827/ • https://www.ncbi.nlm.nih.gov/books/NBK538279/ • https://www.healthline.com/health/informed-consent • https://en.wikipedia.org/wiki/Informed_consent • https://www.sciencedirect.com/