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Barriers in the Process of Achieving Informed Consent From Critically Ill Patients

NCT ID: NCT03405766

Last Updated: 2018-11-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

70 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-05-02

Study Completion Date

2018-11-20

Brief Summary

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The study will explore barriers in the process of achieving informed consent from critically ill patients

Detailed Description

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The barriers will be divided into four major categories:

* Practical barriers
* Medical barriers
* Legal barriers
* Ethical barriers

Conditions

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Critically Ill Ethics Informed Consent Study Recruitment

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Patients considered for inclusion in the NORIDES study

Exclusion Criteria

* None
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Akershus

OTHER

Sponsor Role collaborator

University of Oslo

OTHER

Sponsor Role collaborator

Oslo University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Sigrid Beitland

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Oslo University Hospital

Oslo, , Norway

Site Status

Countries

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Norway

References

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Dahlberg J, Eriksen C, Robertsen A, Beitland S. Barriers and challenges in the process of including critically ill patients in clinical studies. Scand J Trauma Resusc Emerg Med. 2020 Jun 8;28(1):51. doi: 10.1186/s13049-020-00732-x.

Reference Type DERIVED
PMID: 32513204 (View on PubMed)

Other Identifiers

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REK 2017/1254

Identifier Type: -

Identifier Source: org_study_id