ISI assessment in critically ill patients based on the relation of inflammatory response and sleep disorders and its impact on ICU-AW

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2000033894

Enrollment

Unknown

Registered

2020-06-15

Start date

2020-07-01

Completion date

Unknown

Last updated

2020-06-22

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

Conditions

Critically ill

Interventions

case series:Nil

Eligibility

Sex/Gender

All

Age

18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged over 18 years; 2. The patients who are willing to accept the study and sign the informed consent after explanation.

Exclusion criteria

Exclusion criteria: 1. Patients whose cognitive function is not enough to complete emotional, sleep and cognitive tests; 2. Patients taking antidepressants, antipsychotics and drugs that affect cognitive function.

Design outcomes

Primary

Measure	Time frame
severity of insomnia;incidence of ICU-AW;expression level of cytokines;	—

Countries

China

Contacts

Public ContactYamin Yan

Zhongshan Hospital Affiliated to Fudan University

yanyamin12@126.com+86 13671547216

Outcome results

None listed

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