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Long-term Outcomes of Critical Illness Survivors

J

Jian-jun Yang

Status

Unknown

Conditions

Intensive Care Units

Study type

Observational

Funder types

Other

Identifiers

NCT03940755
20190501

Details and patient eligibility

About

The goal of this study is to assess the Long-term Outcomes of Critical Illness Survivors,including physical, psychological, and cognitive sequelae.

Full description

An increasing number of patients survive critical illness; however, the evidence reveals that over the same period the number of patients being sent to rehabilitation settings have tripled . For those who do survive, the latest data indicate that 50-70% of ICU "survivors" will suffer cognitive impairment and 60-80% of "survivors" will suffer functional impairment or ICU-acquired weakness (ICU-AW).Still,there is a lack valid data on the long-term impact on morbidity from prospective observational studies. Therefore, the investigators designed an observational cohort which cover a broader range of outcomes to quantify long-term physical, psychological, and cognitive impairment after intensive care unit (ICU).Intensive Care Unit patients survive from critical illness will be approached for study recruitment and participation.Survival rate,Quality of life,Cognitive impairments,Depression and anxiety,PTSD,Physical activity,Neuromuscular impairment will be assessed 3 or 6 months after ICU discharge.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged >17 years
  • Patients in intensive care unit(ICU) with at least one organ or system dysfunction,such as respiratory failure, cardiogenic shock,or septic shock.

Exclusion criteria

  • Refuse to participate
  • Death before ICU discharge
  • pre-existing cognitive impairment, malignant tumor

Trial design

200 participants in 1 patient group

Critical Illness Survivors
Description:
Those intensive care unit(ICU) patients who survive from critical illness.

Trial contacts and locations

2

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Central trial contact

Ying Li, MD; Jian-jun Yang, PhD

Data sourced from clinicaltrials.gov

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