Study identification

PURI

https://redirect.ema.europa.eu/resource/1000000544

EU PAS number

EUPAS1000000544

Study ID

1000000544

Official title and acronym

Impairment of cognitive, mental and physical functioning in patients after intensive care unit (ICU) stay - Post-intensive care syndrome (PICS-POZ)

DARWIN EU® study

No

Study countries

Poland

Study description

The main objective of the study is to assess the prevalence of PICS syndrome symptoms and their profile (domains) in patients up to 12 months after discharge from the Department of Anesthesiology, Intensive Therapy and Pain Treatment (OAITiLB) of the University Clinical Hospital in Poznań.
The disorders included in the PICS syndrome are expected to occur to varying degrees in most patients admitted to intensive care. Due to the lower availability of intensive care units in Polish hospitals and the associated more severe initial condition of admitted patients, it is likely that PICS syndrome is more common in this population than has been shown in studies conducted in Western countries.

This study was approved by The Bioethical Committee of Poznan University of Medical Sciences (approval No: 703/24 from 6/11/2024)

Study status

Ongoing
Research institutions and networks

Institutions

Department of Anaesthesiology, Intensive Therapy and Paint Treatment, Poznan University of Medical Sciences

Contact details

Szymon Pełczyński

Primary lead investigator
ORCID number:
0000-0003-4070-2034
Study timelines

Date when funding contract was signed

Planned:
Actual:

Study start date

Planned:
Actual:

Data analysis start date

Planned:

Date of final study report

Planned:
Sources of funding
Other public funding (e.g. hospital or university)

More details on funding

Poznan University of Medical Sciences - Doctoral School, Department of Anaesthesiology, Intensive Therapy and Pain Treatment
Study protocol
Initial protocol

Protocol 17.10.2024 PL

English (1.06 MB - PDF)View document
Regulatory

Was the study required by a regulatory body?

No

Is the study required by a Risk Management Plan (RMP)?

Not applicable