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Usage and Adverse Events of Physical Restraints in an Intensive Care Unit

University Hospital Basel logo

University Hospital Basel

Status

Active, not recruiting

Conditions

Physical Restraints

Study type

Observational

Funder types

Other

Identifiers

NCT06921070
2024-00057 am23Sutter;

Details and patient eligibility

About

The aim of this retrospective observational single-center cohort study is to (1) examine the frequency of physical restraint use in a Swiss intensive care unit, (2) identify related adverse events, and (3) determine risk factors associated with their use and complications in critically ill adult patients.

Full description

Physical restraints are widely used in intensive care units (ICU) worldwide to protect patients by preventing them from removing medical devices, accidentally taking out breathing tubes (self-extubation), or falling. However, while they are intended to keep patients safe, restraints can also have negative effects. Their use may increase agitation, self-extubation, infections, blood clots, longer hospital stays, and even a higher risk of death. Studies have also linked physical restraints to long-term problems, such as cognitive decline and post-traumatic stress disorder. However, most studies lack strong evidence and cannot exclude the influence of other factors.

This retrospective observational single-center cohort study aims to:

  1. Determine the frequency with which physical restraints are used in a Swiss ICU
  2. Identify the type and frequency of adverse events associated with physical restraint use
  3. Identify other factors linked to physical restraints use and specific complications during intensive care of critically ill adult patients.

Furthermore, the study examines the use of chemical sedation with physical restraint use and the risk of delirium.

The results of this study will help improve patient care and contribute to better guidelines for physical restraint use in the ICU.

Enrollment

2,000 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients (i.e., patients ≥18 years of age)
  • Being physically restrained in the intensive care unit at the University Hospital Basel between 2010 and 2023

Exclusion criteria

  • Patients younger than 18 years.
  • Patients with documented refusal to use data.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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