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Effect of magnesium sulphate infusion on emergence agitation in patients undergoing video-assisted thoracoscopic lobectomy with general anesthesia

Effect of magnesium sulphate infusion on emergence agitation in patients undergoing video-assisted thoracoscopic lobectomy with general anesthesia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086519
Enrollment
Unknown
Registered
2024-07-04
Start date
2024-07-05
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

lung Cancer

Interventions

Test group:Intravenous infusion of magnesium sulfate 50mg/kg before anesthesia induction
Control group:None

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing video-assisted thoracoscopic lobectomy with general anesthesia; 2. Age 18-65 years old; 3.American Society of Anesthesiologists Physical Status Classification grade I - III; 4.BMI 18-30 kg/m2.

Exclusion criteria

Exclusion criteria: 1. History of mental illness or cognitive dysfunction; 2. Bradycardia and atrioventricular block; 3. preoperative electrolyte disorder; 4. Neuromuscular system diseases; 5. Severe cardiovascular and cerebrovascular diseases, liver, lung and kidney diseases (BUN > 7.5 mmol/L; Scr>110µmol/L); 6. Use polymyxin B sulfate, streptomycin sulfate, calcium gluconate, dobutamine hydrochloride, procaine hydrochloride, penicillin and naftoxacillin (ethoxy) antibiotics; 7. History of drug abuse; 8. Allergy to the drugs involved in this study; 9. Have participated in other clinical studies.

Design outcomes

Primary

MeasureTime frame
Incidence of emergence agitation;

Secondary

MeasureTime frame
Postoperative recovery quality;Extubation time;Postoperative VAS score;Postoperative adverse events;Incidence of rescue analgesia;Usage of analgesic pump within 24 hours after operation;

Countries

China

Contacts

Public ContactChen Xiuxia

Affiliated Hospital of Xuzhou Medical University

cxxlxy@sina.com+86 152 0520 0798

Outcome results

None listed

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