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N/A Completed N=17 Randomized Other

Sleep and Circadian Rhythms in Mechanically Ventilated Patients

Source: ClinicalTrials.gov NCT01276652 ↗
Enrolled (actual)
17
Serious AEs
0.0%
Results posted
Sep 2017
Primary outcomePrimary: Percentage of Subjects Who Successfully Undergo Continuous Bedside Polysomnography for at Least 24 Hours. — 9; 8; 5 Participants

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.

Outcome Measures

OutcomeResultp-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

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. Informational only — not medical advice.

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