- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04344938
Covid 19 Pandemic. Emerging Legal and Ehical Disputes Over Patient Confidentiality
April 15, 2020 updated by: Noha Esmael Ebrahem, Assiut University
Many critical ethical questions arise in pandemic covid 19planning, preparedness and response.
These include: Who will get priority access to medications, vaccines and intensive care unit beds, given the potential shortage of these essential resources?
In the face of a pandemic, what obligations do health-care workers have to work not withstanding risks to their own health and the health of their families?
How can surveillance, isolation, quarantine and social-distancing measures be undertaken in a way that respects ethical norms?
What obligations do countries have to one another with respect to pandemic covid 19 planning and response efforts?
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
874
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
medical and non medical personel
Description
Inclusion Criteria:
- adult aged 18 years to 60 years
- medical personel graduated from egyptian faculty of medicine.
- non medical personel live in egypt
Exclusion Criteria:
- personel less than 18 years old .
- medical personel not graduated from egyptian faculty of medicine.
- non medical personel live outside egypt
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
medical personel
|
Many critical ethical questions arise in pandemic covid 19planning, preparedness and response.
These include: Who will get priority access to medications, vaccines and intensive care unit beds, given the potential shortage of these essential resources?
In the face of a pandemic, what obligations do health-care workers have to work notwithstanding risks to their own health and the health of their families?
How can surveillance, isolation, quarantine and social-distancing measures be undertaken in a way that respects ethical norms?
What obligations do countries have to one another with respect to pandemic covid 19 planning and response efforts?
|
non medical personel
|
Many critical ethical questions arise in pandemic covid 19planning, preparedness and response.
These include: Who will get priority access to medications, vaccines and intensive care unit beds, given the potential shortage of these essential resources?
In the face of a pandemic, what obligations do health-care workers have to work notwithstanding risks to their own health and the health of their families?
How can surveillance, isolation, quarantine and social-distancing measures be undertaken in a way that respects ethical norms?
What obligations do countries have to one another with respect to pandemic covid 19 planning and response efforts?
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Evaluate the ethical requirement of controlled disrupts of patients In case of infectious disease pandemic
Time Frame: 2 months
|
questionaire done to To keep the general preventive measure in the community
|
2 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
April 1, 2020
Primary Completion (Anticipated)
June 1, 2020
Study Completion (Anticipated)
July 1, 2020
Study Registration Dates
First Submitted
April 10, 2020
First Submitted That Met QC Criteria
April 10, 2020
First Posted (Actual)
April 14, 2020
Study Record Updates
Last Update Posted (Actual)
April 17, 2020
Last Update Submitted That Met QC Criteria
April 15, 2020
Last Verified
April 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020A10
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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