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Completed

NCT Number: NCT06339385

Management of PADIS in Emergency Intensive Care Unit

Investigate the prevalence of PADIS in EICU, as well as the awareness and clinical implementation status of medical staff towards PADIS.

The investigators conducted a multicenter cross-sectional survey in mainland China, including a one-day point prevalence investigation and a questionnaire survey. The inclusion criteria encompassed all adult patients admitted to the participating emergency department intensive care units (EDICUs) during the on-site screening, while exclusion criteria comprised patients aged less than 18 years, EDICU stays duration less than 24 hours before the screening, and participation in other concurrent trials. Hospital and nursing records from the 24 hours preceding enrollment were examined to document the assessment rate of pain, agitation-sedation, and delirium. Physicians and nurses on duty 24 hours before the patients' enrollment was invited to complete the questionnaire survey regarding the ICU profiles, professional expertise, assessment and treatment of PAD, early mobilization, and sleep improvement practices.

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Key information

Conditions

Pain Agitation, Emergence Confusion Critical Illness Delirium Disease Attributes Emergence Delirium Mental Disorders Nervous System Diseases Neurobehavioral Manifestations Neurocognitive Disorders Neurologic Manifestations Pathologic Processes Pathological Conditions, Signs and Symptoms Postoperative Complications Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Beijing Tiantan hospital

Beijing, Beijing Municipality, 100070, China

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • All patients admitted to the participating EDICU during the on-site investigation

Exclusion criteria

  • Age less than 18 years;
  • EDICU stay duration before the screening was less than 24 hours
  • Enrollment in other concurrent trials.

Treatment and study plan

PADIS assessment

Behavioral

Hospital and nursing records from the 24 hours preceding enrollment were examined to document the assessment rate of pain, agitation-sedation, and delirium.

Primary outcomes

  1. PADIS assessment rate

    Time frame: 24 hours before enrollment

Secondary outcomes

  1. Rates of analgesic and sedative administration

    Time frame: 24 hours before enrollment

  2. Rate of accidental removal of the catheter during the EICU stay

    Time frame: From the start of the survey day until transfer out of the EDICU or 60 days after the survey day.

  3. EDICU length of stay

    Time frame: From the start of the survey day until transfer out of the EDICU or 60 days after the survey day.

  4. The hospital length of stay

    Time frame: From the start of the survey day until transfer out of the EDICU or 60 days after the survey day.

Sponsors and collaborators

Lead sponsor

Capital Medical University

Other

Collaborators

  • Beijing Anzhen Hospital
  • Beijing Tiantan Hospital
  • Fudan University
  • General Hospital of Shenyang Military Region
  • Guilin Medical University, China
  • Jiangxi Provincial People's Hopital
  • Mianyang Central Hospital
  • Southwest Hospital, China
  • The First Affiliated Hospital of Anhui Medical University
  • The First Affiliated Hospital of Dalian Medical University
  • The First Affiliated Hospital of Zhengzhou University
  • The First Hospital of Hebei Medical University
  • The First Hospital of Jilin University
  • The Second Affiliated Hospital of Hainan Medical University
  • Tianjin Medical University General Hospital

Registry information

Official study title

Management of Pain, Agitation-sedation, Delirium Immobility and Sleep Disruption in Emergency Intensive Care Unit: a Multicenter Cross-sectional Survey

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Apr 1, 2024
Registry last updated
Apr 2, 2024

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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