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Completed

NCT Number: NCT03194360

Risk Factors of Delirium in Sequential Sedation Patients in Intensive Care Unit

Delirium is one of main adverse events in ventilated patients who receive long-term usage of mono-sedative. Sequential sedation may reduce these adverse effects. This study aimed to evaluate incidence and risk factors for delirium in sequential sedation patients.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Critical care medicine of West China Hospital

Chengdu, Sichuan, 610041, China

About this study

Previous studies have showed that patients under mechanical ventilation have a higher risk for experiencing delirium than nonmechanically ventilated patients (20%-50%). Its occurrence is also more frequent in elder patients. More than that, it is often hard to identify delirium by physicians, leading to unreasonable management of ICU patients.

And delirium is one of main adverse events in ventilated patients who receive long-term usage of mono-sedative. Sequential sedation may reduce these adverse effects.

However, few present studies focus on delirium in sequential sedation patients. Thus, in this study, we aimed to determine the factors of delirium in patients who received sequential sedation in ICU.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Intubated patients;
  • Age≥18 years old;
  • Anticipated Ventilation and sedation duration of at least 72 hours.

Exclusion criteria

  • Allergy to the study drug;
  • suspected pregnancy;
  • gross obesity;
  • Extremely unstable of circulatory system, such as systolic blood pressure less than 90 mm Hg despite plasma volume expansion and continuous infusions of vasopressors before the start of study drug infusion;
  • Uncontrolled abnormal hypertension, such as systolic blood pressure more than 180 mmHg or diastolic more than105 mmHg;
  • Heart rate less than 50 bpm;
  • Second or third degree heart block;
  • moribund state;
  • history of alcoholism or intake of anti-anxiety drugs or hypnotics;
  • chronic renal failure;
  • coma by cranial trauma or neurosurgery or unknown etiology or epileptic state;
  • History of neuromuscular disease;
  • unwillingness to provide informed consent by patients or their authorized surrogates following ICU admission.

Treatment and study plan

Primary outcomes

  1. Delirium assessment in Sequential Sedation Patients

    Time frame: A maximum of twenty-eight days or until ICU discharge, whichever occurred first.

    The primary outcome of this study was delirium. Patient evaluations were implemented using Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) scale every four hours a day for a maximum of twenty-eight days or until ICU discharge, whichever occurred first. The risk factors were analyzed using risk regression (logistic-regression). Any variables which had P<0.2 after univariable logistic-regression or potential variables associated with delirium were included for multivariable logistic-regression. P<0.05 was considered to represent statistical significance.

Sponsors and collaborators

Lead sponsor

West China Hospital

Other

Registry information

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
Jun 21, 2017
Registry last updated
Jun 21, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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