Study on the construction of visualization evaluation system for acquired weakness in critical illness

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2300075581

Enrollment

Unknown

Registered

2023-09-08

Start date

2023-08-28

Completion date

Unknown

Last updated

2023-09-11

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

Conditions

acquired weakness in critical illness

Interventions

Case series:none

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Age>18 years old 2. Estimated patient hospitalization time>3 days 3. Willing to accept this experiment and sign an informed consent form

Exclusion criteria

Exclusion criteria: 1. Patients who are unable to obtain ultrasound images of muscle fat; 2. Patients with incomplete clinical data; 3. Having primary motor dysfunction or clear neuromuscular diseases; 4. Lumbar spine, pelvis, lower limb trauma or surgery; 5. Limb defects; 6. Redness, swelling, bleeding, etc. at the measurement points of both lower limbs; 7. Expect death or seek palliative treatment.

Design outcomes

Primary

Measure	Time frame
ICU hospitalization time;patient outcomes;ICU hospitalization expenses;	—

Secondary

Measure	Time frame
Long term survival;quality of life;Self-care ability;cognitive ability;	—

Countries

CHINA

Contacts

Public ContactWANHONG YIN

West China Hospital of Sichuan University

yinwanhong@wchscu.cn+86 135 1810 6758

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 28, 2026