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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03405766
Enrollment
70
Registered
2018-01-23
Start date
2018-05-02
Completion date
2018-11-20
Last updated
2018-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Critically Ill, Ethics, Informed Consent, Study Recruitment

Brief summary

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

Detailed description

The barriers will be divided into four major categories: * Practical barriers * Medical barriers * Legal barriers * Ethical barriers

Interventions

None listed

Sponsors

University Hospital, Akershus
CollaboratorOTHER
University of Oslo
CollaboratorOTHER
Oslo University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients considered for inclusion in the NORIDES study

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Study recruitment barriers, Medical2018-2022Number (%) of patients unable to give consent or to sign
Study recruitment barriers, Ethical2018-2022Number (%) of patients not asked to give consent due to ethical issues

Secondary

MeasureTime frameDescription
Study recruitment barriers, Practical2018-2022Number (%) of cases where practical reasons made consent impossible
Study recruitment barriers, Legal2018-2022Number (%) of patients where legal issues made consent impossible

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026