N/A N=17 Randomized Other

Sleep and Circadian Rhythms in Mechanically Ventilated Patients

Respiratory Failure · Critical Illness

Bottom Line

View on ClinicalTrials.gov: NCT01276652 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Sep 2017

Primary outcome: Primary: Percentage of Subjects Who Successfully Undergo Continuous Bedside Polysomnography for at Least 24 Hours. — 9; 8; 5 Participants

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Environmental modification (Behavioral)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: University of Iowa
Primary completion: Dec 2008

Outcome Measures

Outcome	Result	p-value
PRIMARY Percentage of Subjects Who Successfully Undergo Continuous Bedside Polysomnography for at Least 24 Hours.	9; 8; 5	—
SECONDARY Subject Tolerance of the Environmental Modification Protocol	9	—

Summary

This study examines the feasibility of assessing sleep and circadian rhythmicity in critically ill patients undergoing mechanical ventilation. Secondarily, it will examine the feasibility of reducing subject exposure to environmental light and noise and of delivering routine care according to classical day/night routines.

Eligibility Criteria

Inclusion Criteria

Adults undergoing mechanical ventilation in the medical intensive care unit.

Exclusion Criteria

Central nervous system disease (stroke, seizure, dementia, etc)
Metabolic or hypoxic encephalopathy
Confirmed or suspected drug overdose
Currently receiving neuromuscular blockers
Coma

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01276652). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.