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The influence and significance of NE continuous infusion combined with GDHT on intraoperative and postoperative outcomes in patients with brain tumor resection

The influence and significance of NE continuous infusion combined with GDHT on intraoperative and postoperative outcomes in patients with brain tumor resection

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084337
Enrollment
Unknown
Registered
2024-05-14
Start date
2024-02-22
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Patients with brain tumor, meningioma and hemangioma

Interventions

Experimental groups:Continuous infusion of norepinephrine combined with GDHT regimen
control groups:bolus of norepinephrine combined with GDHT regimen

Sponsors

the First Affiliated Hospital of Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who are selected to undergo resection of brain tumor, meningioma and hemangioma. 2. Surgical duration>3 hours. 3. Patients aged>18 years old. 4. The patient is able to understand the written informed consent document and has the willingness to sign it.

Exclusion criteria

Exclusion criteria: 1. Patients with tumors located in the brainstem and deep brain stem. 2. Patients aged = 18 years old 3. Patients with ASA grading>Level III 4. Patients with a body mass index (BMI) greater than 30 kg/m2 or less than 15 kg/m2 5. Patients with preoperative arrhythmia or newly developed arrhythmia after anesthesia induction. 6. Patients with moderate to severe heart valve disease. 7. Patients with preoperative ventricular dysfunction (left ventricular ejection fraction<40%, right ventricular dysfunction, intracardiac shunt). 8. Patients with preoperative hemodynamic instability. 9. Patients with preoperative sepsis. 10.Patients with chronic kidney disease and a glomerular filtration rate of<30 ml/min/1.73m^2 or requiring renal replacement therapy.

Design outcomes

Primary

MeasureTime frame
systemic inflammatory response syndrome (SIRS) and dysfunction of at least one major organ system;

Secondary

MeasureTime frame
liquid intake and outflow;Time spent in the ICU;

Countries

China

Contacts

Public ContactKe An

the First Affiliated Hospital of Sun Yat-Sen University

anke@mail.sysu.edu.cn+86 158 0003 7306

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026