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Comparison of Prognosis Between Intracranial Pressure Centered Monitoring Methods and Multimodal Monitoring Methods in Patients with Moderate to Sever Traumatic Brain Injury

Comparison of Prognosis Between Intracranial Pressure Centered Monitoring Methods and Multimodal Monitoring Methods in Patients with Moderate to Sever Traumatic Brain Injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123080
Enrollment
Unknown
Registered
2026-04-21
Start date
2022-07-15
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Moderate to Severe Traumatic Brain Injury

Interventions

Multimodal Monitoring Group:Insert ICP probe during surgery, monitor CPP, cerebral oxygenation (NIRS), brain temperature, and TCD postoperatively, record sedation and analgesia depth using BIS
implement interventions (including hypothermia therapy) based on ICP, CPP, cerebral oxygenation, brain temperature, and TCD
ICP Monitoring Group:Insert ICP probe during surgery, monitor CPP and ICP within 24 hours postoperatively, implement interventions based on ICP and CPP, record sedation and analgesia depth using BIS

Sponsors

Changzhou No.2 People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Over 18 years old.; 2. Admitted to the hospital due to non-penetrating craniocerebral trauma and implanted with an intracranial pressure probe.; 3. Preoperative GCS score <=12 points without sedation and analgesia.; 4. All patients were diagnosed by cranial CT examination upon admission.

Exclusion criteria

Exclusion criteria: 1. Patients with an estimated total hospital stay of no more than 2 days. 2. Preoperative GCS score =3 points, or fixed and dilated pupils. 3. Before this injury, due to various conditions such as trauma, spinal cord diseases, stroke, etc., the patient's original limb movement, language function, etc. were already restricted, such as hemiplegia, unclear speech, etc., affecting the patient's functional score.

Design outcomes

Primary

MeasureTime frame
Survival situation;Postoperative GOS scores at 1, 3, and 6 months;Postoperative BI scores at 1, 3, and 6 months;

Secondary

MeasureTime frame
ICU length of stay;Total hospitalization length of stay;Complications;Mechanical ventilation duration;Tracheostomy;Sedative duration;Analgesic duration;Use of lytic cocktail;Total hospitalization costs;Reoperation;

Countries

China

Contacts

Public ContactLiu Fang

Changzhou No.2 People’s Hospital

czdoctorliu@hotmail.com+86 159 5122 8543

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026