Clin2
NCT05783505Possibly a fitRecruiting

Program to calm ICU patients and reduce restraints

Agitation,Psychomotor

Part of Brain & nervous system clinical trials.

This study tests a multi-step program to prevent and lessen agitation in ICU patients, with the goal of reducing the need for physical restraints. It also aims to improve comfort and safety during a longer ICU stay.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
480 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are an adult (18 years or older).
  • Your ICU stay is expected to last more than 24 hours.
  • You are likely to become agitated (restless, confused, or upset) within the first 14 days in the ICU.
  • You can be considered for a specific calming medicine (dexmedetomidine), without key heart-blood-pressure or allergy problems.
  • You are not on ECMO (a heart-lung machine).
  • You have not joined another sedation study, and consent is available for long-term follow-up in MONITOR-IC.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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