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Clinical application of non-invasive multimodality monitoring equipment in postoperative monitoring of children with craniocerebral injury

Clinical application of non-invasive multimodality monitoring equipment in postoperative monitoring of children with craniocerebral injury

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100045057
Enrollment
Unknown
Registered
2021-04-04
Start date
2021-04-01
Completion date
Unknown
Last updated
2021-11-08

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

Conditions

Craniocerebral injured patient

Interventions

control group:None
craniocerebral injury group:None

Sponsors

Children's Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 16 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 0 and 16 years with no restriction on sex; 2.Recovering from surgical treatment for craniocerebral injury; 3.Complete skull, no wound near the wing point or above the brow arch or the diameter of the puncture wound is less than 2 cm, and if decompressive craniectomy is performed, the monitor should conduct after the bone flaps be replaced and sutured for 2 days.

Exclusion criteria

Exclusion criteria: 1.Metal implants in the skull; 2.Dermatosis in the head and neck affecting electrode stickers; 3.Anaphylaxis to electrode stickers heavily; 4.Patients with delirium or mental disorders.

Design outcomes

Primary

MeasureTime frame
Disturbance coefficient;Cerebral tissue oxygen saturation;—

Countries

China

Contacts

Public ContactXu Feng

Intensive Care Unit, Children's hospital of Chongqing Medical University

xufeng9899@163.com+86 15320206699

Outcome results

None listed

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