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The effects of nimodipine on postoperative cognitive dysfunction in patients with traumatic brain injury undergoing non craniocerebral surgery

The effects of nimodipine on postoperative cognitive dysfunction in patients with traumatic brain injury undergoing non craniocerebral surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17013575
Enrollment
Unknown
Registered
2017-11-28
Start date
2017-12-01
Completion date
Unknown
Last updated
2017-12-11

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

Conditions

traumatic brain injury

Interventions

control group:Standard treatment
Nimodipine group:treatment of nimodipine

Sponsors

the Third Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients with traumatic brain injury receiving non craniocerebral operation under general anesthesia, American Society of Anesthesiologists' physical status classes I & II; 2. no history of neurological diseases and alcohol abuse; 3. no severe vision or hearing impairment and no obvious abnormality of heart, lung, liver and kidney function.

Exclusion criteria

Exclusion criteria: (1) Operation time is longer than 3 hours; (2) The intraoperative blood loss is more than 800ml; (3) The operation is cancelled for various reasons

Design outcomes

Primary

MeasureTime frame
s100ß;GFAP;—

Countries

China

Contacts

Public ContactQiujun Wang

the Third Hospital of Hebei Medical University

13933178001@163.com+86 18533112929

Outcome results

None listed

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