Study on the improvement of neurological function and prognosis of ERAS in the perioperative period of brain injury

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000036485

Enrollment

Unknown

Registered

2020-08-23

Start date

2020-10-01

Completion date

Unknown

Last updated

2020-09-14

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

Conditions

brain injury

Interventions

Experimental group:Enhanced recovery after surgery

Control group:regular treatment

Eligibility

Sex/Gender

All

Age

15 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Perioperative patients with brain tumour,cerebral hemorrhage,cerebral infarction and brain trauma; 2. Aged between 15 to 75 years old, male or female; 3. Able to understand and complete this training; 4. Willing to sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Coma patients; 2. Emergency surgery patients; 3. Unable to follow-up; 4. Unstable Vital Signs.

Design outcomes

Primary

Measure	Time frame
psychological assessment;cognitive function assessment;motor function assessment;speech function assessment;swallowing function assessment;pain;	—

Secondary

Measure	Time frame
fMRI or DTI;	—

Countries

China

Contacts

Public ContactYulian Zhu

Huashan Hospital, Fudan University

hsyykfkzyl@163.com+86 13816783039

Outcome results

None listed

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