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The Very Old Intensive Care Patient: A Multinational Prospective Observation Study

The Very Old Intensive Care Patient: A Multinational Prospective Observation Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03134807
Acronym
VIP1
Enrollment
5132
Registered
2017-05-01
Start date
2016-11-01
Completion date
2017-10-31
Last updated
2018-05-15

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

Conditions

Critical Illness, Old Age; Debility, Survival

Brief summary

* The primary aim is to document the incidence and short-term outcome of the elderly ICU patient (≥ 80 years) using a multicentre, multi national approach * The secondary aim is to investigate the properties of a simple frailty index in this cohort, and in particular if this is an instrument that can be used in resource and outcome prediction in this group * To create hypothesis for further studies, in particular on various outcome prediction

Detailed description

The investigators have chosen to use a prospective registration of routinely collected data in this ICU population. The study is mainly European based, but will also allow for ICUs outside Europe to participate. 20 consecutive ICU admission in patients ≥ 80 years of age will be collected OR all patients ≥ 80 years in a three months' period (whatever comes first). Data are collected electronically through an e-CRF and with baseline documentation of the ICU. The database is located in Denmark, at the Department of Epidemiology, University of Aarhus (http://vip1study.com/) . Each ICU will only have access through the database of their own patients, and patient ID is not registered (Names, birth-date or social security numbers) so it is in that sense anonymous. Even with de-identified data, most countries must seek necessary consent from the authorities to collect such data, and hence there will be a period between ICU recruitment (starting April 2016) and patient recruitment (October 1. 2016) to allow for this to be done prior to study start. The goal is to recruit at least 100 ICUs which will give data from approximately 2000 elderly patients.

Interventions

OTHERObservation prospective

No intervention

Sponsors

European Society of Intensive Care Medicine
CollaboratorOTHER
University of Bergen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* All admissions in the group

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Survival30 daysICU and 30 days
FrailtyPre admissionClinical Frailty Scale

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 9, 2026