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The effect of critical-care pain observation (CPOT) utilizaiton in the communicative disorders adult patient in the Intensive Care Unit (ICU)

The effect of critical-care pain observation (CPOT) utilizaiton in the communicative disorders adult patient in the Intensive Care Unit (ICU)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100045036
Enrollment
Unknown
Registered
2021-04-03
Start date
2020-08-01
Completion date
Unknown
Last updated
2021-11-08

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

Conditions

communication disorders

Interventions

Intervention group:Critical-care pain observation (CPOT)
Control group:Facial expression pain rating scale (FPS-R)

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.ICU patients; 2.Aged over 18 years; 3.Communication disorders (mechanical ventilation: non-mechanical ventilation: RASS score -4~+1 or total GCS score was 3~14).

Exclusion criteria

Exclusion criteria: 1.Neuromuscular blockers or Hibernation mixture treatment; 2.Diagnosed myasthenia gravis or brain death; 3.No limb function (quadriplegia or GCS motor response score was 1); 4.Terminal situation; 5.Participate in other intervention study.

Design outcomes

Primary

MeasureTime frame
Analgesia dosage;Total sedative dosage;Length of ICU stay;Demographic data Questionnaire;—

Secondary

MeasureTime frame
Time of Mechanical Ventilation;Length of ICU stay;—

Countries

China

Contacts

Public ContactFang Fang
fang_fang0604@163.com+86 13386259592

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026