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Falls Of Unknown Origin (FUKNO) - Are Morbidity and Mortality Predictable in Patients Presenting With Falls?

Falls Of Unknown Origin (FUKNO) - Are Morbidity and Mortality Predictable in Patients Presenting With Falls?

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02244983
Acronym
FUKNO
Enrollment
587
Registered
2014-09-19
Start date
2014-11-12
Completion date
2021-12-02
Last updated
2022-07-21

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

Conditions

Accidental Falls, Underlying Disease of Falls

Brief summary

It is the investigators goal to identify the prevalence of underlying diseases, make disposition more rational, and establish risk stratification tools in elderly patients presenting with falls. Additionally, the outcome of standard care (clinical assessment only for disposition) will be compared with a new approach combining the standard of care with biomarker assisted disposition of elderly patients presenting with falls. Therefore the investigators are looking at the following points. Emergency department work-up 1. Prevalence of underlying disease 2. Developing algorithms for initial assessment Disposition a. Establishing biomarker enhanced disposition planning by using risk-stratification tools b. Comparing geriatric emergency assessment to standardized disposition planning

Interventions

OTHERPatients History

History taking and drawing of a blood sample

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* All fall patients aged 65 years and older who presented to the emergency department giving written informed consent

Exclusion criteria

* Patients below 65 years * Non-fall patients above 65 years * or lack of informed consent by patients or proxies

Design outcomes

Primary

MeasureTime frameDescription
Mortality30 DaysData Collection via Case Report Form

Secondary

MeasureTime frameDescription
Acute Morbidity30 DaysData Collection via Case Report Form
Institutionalisation180 DaysData Collection via interview with general practitioner
Disposition30 DaysData collection via case report form
Mortality90 DaysData Collection via Case Report Form

Countries

Germany, Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026