HMP 501 Designing Clinical Trial Treatment or Vaccine Solution

HMP 501 Designing Clinical Trial Treatment or Vaccine

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HMP 501 Designing Clinical Trial Treatment or Vaccine

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Randomized controlled trials are typically considered to be the gold standard of clinical research. However, when research is conducted during an emergency, alternative trial designs might be more appropriate, for example, a design in which every participant receives the experimental treatment or vaccine, in the hope that it will provide some benefit. What ethical

considerations are relevant to designing a clinical trial of a treatment or vaccine in the midst of the COVID-19 pandemic?

Assessment of Acute Kidney Rejection Abstract

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HMP 501 Designing Clinical Trial Treatment or Vaccine

Research abstract for an ongoing project It is called assessment of acute kidney rejection using urinary and plasma signatures in Saudi patients.

abstract for an ongoing research project it is called assessment of acute kidney rejection using urinary and plasma signatures in Saudi transplant patients. So the total of patient right now 140- 2 years so far but the research is 5 years and looking for 450 patients. What we have done so far we collected blood and urine from patients ( we did not take saliva so far-

it was meant for babes that if we cannot take blood we can extract DNA or RNA from the saliva). There are different project under this 1- with the proteomics ( the department of proteomics took the plasma after we did PBMCs test to separate the blood. ) 2- genetics ( they took DNA to run Exome known as whole genome sequencing and axiom tests for “ The

Saudi genome project”. 3- RNA for gene expressions 4- urine both RNA and Urine were collected and they will be send to one collaborator in US. Part of the paper we are looking for is the history of the family so we wrote a map on a board “ see the picture”. So we contacted with the patient or went to their hospital history to find the info that was written in the board . S

HMP 501 Designing Clinical Trial Treatment or Vaccine

RUBRIC
Excellent Quality 95-100%	Introduction 45-41 points The background and significance of the problem and a clear statement of the research purpose is provided. The search history is mentioned.		Literature Support 91-84  points The background and significance of the problem and a clear statement of the research purpose is provided. The search history is mentioned.			Methodology 58-53 points Content is well-organized with headings for each slide and bulleted lists to group related material as needed. Use of font, color, graphics, effects, etc. to enhance readability and presentation content is excellent. Length requirements of 10 slides/pages or less is met.
Average Score 50-85%	40-38 points More depth/detail for the background and significance is needed, or the research detail is not clear. No search history information is provided.		83-76  points Review of relevant theoretical literature is evident, but there is little integration of studies into concepts related to problem. Review is partially focused and organized. Supporting and opposing research are included. Summary of information presented is included. Conclusion may not contain a biblical integration.			52-49  points Content is somewhat organized, but no structure is apparent. The use of font, color, graphics, effects, etc. is occasionally detracting to the presentation content. Length requirements may not be met.
Poor Quality 0-45%	37-1 points The background and/or significance are missing. No search history information is provided.		75-1 points Review of relevant theoretical literature is evident, but there is no integration of studies into concepts related to problem. Review is partially focused and organized. Supporting and opposing research are not included in the summary of information presented. Conclusion does not contain a biblical integration.			48-1 points There is no clear or logical organizational structure. No logical sequence is apparent. The use of font, color, graphics, effects etc. is often detracting to the presentation content. Length requirements may not be met
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