Establishment of prediction model for postoperative delirium patients and study of metabolomics and proteomics

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2100046411

Enrollment

Unknown

Registered

2021-05-15

Start date

2021-06-02

Completion date

Unknown

Last updated

2022-01-04

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

Conditions

Postoperative Cognition Dysfunctionn

Interventions

Non-delirium Group:None

Delirium Group :None

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged over 18 years; 2. Patients after elective surgery; 3. CAM scale Nu.DESC scale confirmed delirium patients; 4. CAM scale Nu.DESC scale for non-delirium patients; 5. Sign the informed consent form voluntarily.

Exclusion criteria

Exclusion criteria: 1. Serious adverse cardiovascular events occurred during the operation; 2. Transfer to ICU immediately after surgery; 3. Communication barriers, unable to cooperate with researchers, such as language comprehension barriers, mental illness, etc.; 4. Severe cardiovascular and cerebrovascular diseases.

Design outcomes

Primary

Measure	Time frame
proteomics research;metabolomics research;	—

Countries

China

Contacts

Public ContactZhang Wei

He'nan Provincial People's Hospital

myhope2005@163.com+86 13838299702

Outcome results

None listed

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