- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03421171
Ethical Dilemmas in Anaesthesiology in the Netherlands; a Qualitative Interview Study. (AnaesthEthics)
January 29, 2018 updated by: E.A. Kwofie, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
This study will describe which ethical dilemmas are experienced by anesthesiologist in the Dutch Healthcare system and what the current solving strategies are for these issues.
Semi- structured interviews will be conducted with anaesthesiologists employed in different hospitals in the Netherlands..
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Ethical considerations are part of a doctors daily practice.
The development of anaesthesiologists as ' perioperative' doctors is increasingly giving anaesthesiologists a treatment function.
As the third largest medical specialty, they are also involved in ethical dilemmas.
Examples of common themes in the literature include:' informed consent' and professionalism.
Nevertheless, good research into ethical dilemmas in the field of anaesthesiology is lacking.
Study Type
Observational
Enrollment (Anticipated)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: E A Kwofie
- Phone Number: 0031 06 11373823
- Email: e.a.kwofie@amc.uva.nl
Study Locations
-
-
-
Amsterdam, Netherlands, 1105 AZ
- Recruiting
- Academic Medical Centre
-
Contact:
- E A Kwofie, drs
- Phone Number: 0031 611 373823
- Email: e.a.kwofie@amc.uva.nl
-
-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
anaesthetist employed in the Netherlands working in a academic of non-academic hospital.
Description
Inclusion Criteria:
- Participant is willing and able to give informed consent for participation in the study.
- Employed as anaesthesiologist
- Employed in an academic or non-academic hospital in the Netherlands
Exclusion Criteria:
- Other medical specialists
- language barrier
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
- Observational Models: Other
- Time Perspectives: Other
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
interviews (qualitative interview study)
Time Frame: 10 years (depends on working experience of the respondent)
|
Categories of ethical dilemmas experienced during work as assessed by interviews
|
10 years (depends on working experience of the respondent)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: M. W Hollmann, AIDS Malignancy Consortium
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 (Actual)
January 20, 2018
Primary Completion (Anticipated)
December 20, 2018
Study Completion (Anticipated)
January 20, 2019
Study Registration Dates
First Submitted
January 23, 2018
First Submitted That Met QC Criteria
January 29, 2018
First Posted (Actual)
February 5, 2018
Study Record Updates
Last Update Posted (Actual)
February 5, 2018
Last Update Submitted That Met QC Criteria
January 29, 2018
Last Verified
January 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- AE1-AMC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
IPD Plan Description
De identified individual participant data for all primary and secondary outcome measures will be made available
IPD Sharing Time Frame
within 6 months of study completion
IPD Sharing Access Criteria
data acces will be reviewed.
requestors will be required to sign a data access agreement
IPD Sharing Supporting Information Type
- Study Protocol
- Statistical Analysis Plan (SAP)
- Clinical Study Report (CSR)
- Analytic Code
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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