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Practice of Sedation and Analgesia in Patients With Severe Brain Injury in China

A Survey on the Practice of Sedation and Analgesia Among Patients With Severe Brain Injury in China: a Prospective Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03975751
Enrollment
387
Registered
2019-06-05
Start date
2019-01-08
Completion date
2019-03-09
Last updated
2019-06-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intensive Care Unit

Keywords

severe brain injuries, sedation and analgesia, intensive care unit, survey

Brief summary

Sedation and analgesia is necessary management for patients in the intensive care units. The high-level studies of sedation and analgesia in China are still deficient, especially in patients with brain injuries who even have been excluded from the relevant studies.

Detailed description

Sedation and analgesia is necessary management for patients in the intensive care units. The high-level studies of sedation and analgesia in China are still deficient, especially in patients with brain injuries who even have been excluded from the relevant studies. In the present study, a multicenter, 1-day point cross-sectional study about the sedation and analgesia among patients in China, particularly brain-injured will be investigated. The objectives are to investigate sedation and analgesia among patients in China and to compare sedation and analgesia between brain injuries and other patients.

Interventions

DIAGNOSTIC_TESTThe Glasgow Coma Scale (GCS)

Use the common GCS, RASS and self-reported pain assessment for evaluating consciousness, agitation/sedation and analgesia.

Sponsors

Capital Medical University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All adult patients admitted to the participating ICUs on the investigation day

Exclusion criteria

* Age under 18 years * Less than 24 hours of ICU stay before screening * Taking part in other studies

Design outcomes

Primary

MeasureTime frameDescription
Performance of sedation assessmentThe previous 24 hours prior to the on-site investigationThe percentage of patients receiving sedation assessment
Performance of pain assessmentThe previous 24 hours prior to the on-site investigationThe percentage of patients receiving pain assessment

Secondary

MeasureTime frameDescription
Use of sedativesThe previous 24 hours prior to the on-site investigationThe percentage of patients receiving sedatives
Use of analgesicsThe previous 24 hours prior to the on-site investigationThe percentage of patients receiving analgesics
ICU mortalityWithin 60 days after on-site investigationThe percentage of patients dead in the ICU
Hospital mortalityWithin 60 days after on-site investigationThe percentage of patients dead in the hospital

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026