Study on the application of TPU and PLA external AIDS to the evaluation and treatment of brain function

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300078630

Enrollment

Unknown

Registered

2023-12-14

Start date

2023-12-14

Completion date

Unknown

Last updated

2023-12-19

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

Conditions

Cranial defect

Interventions

Experimental Group A:Routine rehabilitation training + wear TPU external AIDS for skull defects+ rTMS

Control Group:Routine rehabilitation training

Experimental Group B:Routine rehabilitation training + wear PLA external AIDS for skull defects+ rTMS

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1: The subjects had complete data. 2: The diagnosis met the diagnostic criteria for craniocerebral trauma. Due to various reasons, bone flap removal was needed to save life, and all of them received craniocerebral hematoma drainage treatment.

Exclusion criteria

Exclusion criteria: There are metal foreign bodies in the skull, cardiac pacemakers, heart stents, cochlear implants, intracranial pressure significantly increased, intracranial infection, acute stage of cerebral hemorrhage, etc.

Design outcomes

Primary

Measure	Time frame
fNIRS;	—

Countries

China

Contacts

Public ContactLongwen He

Shanghai Hebin Rehabilitation Hospital

18018880577@163.com+86 180 1888 0577

Outcome results

None listed

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