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Clinical study of standard indication of decompressive craniectomy for TBI based on multimodal monitoring technology

Clinical study of standard indication of decompressive craniectomy for TBI based on multimodal monitoring technology

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100041748
Enrollment
Unknown
Registered
2021-01-04
Start date
2021-01-31
Completion date
Unknown
Last updated
2021-03-22

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

Conditions

Traumatic Brain Injury

Interventions

Single Group:N.A.

Sponsors

The First Affiliated Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (a) TBI patients confirmed with elevated ICP needing craniotomy according to pre-operational assessment. (b) Patients' age between 16 and 75 years old. (c) Patients or his/her authorized representor accepted to be included. (d) Bone flap was replaced back according to the given standard.

Exclusion criteria

Exclusion criteria: (a) Patients with life-threatening disease before TBI events. (b) Patinets with severe neurological disease or defect before TBI events. (c) Patients unsuitable for surgery. (d) Patients with open craniocerebral injury. (e) Patients already within decompensation stage of shock or suffered from more than 30-minute cardiorespiratory arrest.

Design outcomes

Primary

MeasureTime frame
Post-Operational ICP;—

Secondary

MeasureTime frame
GOS (6 month);Overall cost;—

Countries

China

Contacts

Public ContactWen Liang

The First Affiliated Hospital, Zhejiang University School of Medicine

wenliang@zju.edu.cn+86 13575777664

Outcome results

None listed

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