Skip to content

Effect of Intraoperative Dynamic Infusion of Norepinephrine Combined with Restrictive Delayed Fluid Administration on Postoperative Pulmonary Complications in Elderly Patients Undergoing Thoracoscopic Surgery: A Double-Blind, Randomized, Controlled Trial

Effect of Intraoperative Dynamic Infusion of Norepinephrine Combined with Restrictive Delayed Fluid Administration on Postoperative Pulmonary Complications in Elderly Patients Undergoing Thoracoscopic Surgery: A Double-Blind, Randomized, Controlled Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105679
Enrollment
Unknown
Registered
2025-07-09
Start date
2025-07-09
Completion date
Unknown
Last updated
2025-07-14

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

Conditions

Postoperative pulmonary complications

Interventions

Control group :Goal-directed fluid therapy
Experimental group:Low-dose norepinephrine combined with restrictive deferred hydration

Sponsors

Affiliated Cancer Hospital and institute of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1)Age >= 65 years old (2)ASA physical status classification: I to III (3)Undergoing VATS under general anesthesia with bronchial intubation, including pulmonary segmentectomy, lobectomy, sleeve resection, and pneumonectomy (4)Expected surgical duration >= 2 hours, Expected postoperative hospital stay >= 2 days (5)With good cardiopulmonary function and no obvious surgical contraindications (6)Body mass index (BMI) >= 18 kg/m^2 and <= 30 kg/m^2 (7)Voluntarily participation and signed the informed consent

Exclusion criteria

Exclusion criteria: (1)Pre-existing pulmonary diseases that affect the measurement of key observation indicators before surgery (such as acute respiratory distress syndrome (ARDS), pulmonary embolism, pleural effusion, cardiogenic pulmonary edema, pneumothorax, bronchospasm, etc.). (2)Conversion to thoracotomy (3)Allergy to any general anesthetic agents, including propofol, sufentanil, remifentanil, etc. (4)Allergy to norepinephrine (5)Patients with intracranial hypertension, glaucoma, or hyperthyroidism (6)Patients with poor general condition, combined with a history of severe cardiovascular, respiratory, hepatorenal, central nervous system diseases, or extensive tumor metastasis, and with a life expectancy potentially less than 3 months (7)History of dementia, psychiatric disorders, or other neurological diseases

Design outcomes

Primary

MeasureTime frame
postoperative pulmonary complications;

Secondary

MeasureTime frame
Incident acute kidney injury (AKI);Incident dialysising;15-item Quality of Recovery (QoR-15) scale score;Length of Stay;Unplanned admission to intensive care unit (ICU);Creatinine,lactate levels;

Countries

China

Contacts

Public ContactYao Yonghua

Affiliated Cancer Hospital and institute of Guangzhou Medical University

1575041594@qq.com+86 20 6667 3666

Outcome results

None listed

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