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Clinical application of esketamine combined with magnesium sulfate in postoperative analgesia of laparoscopic gynecological surgery

Clinical application of esketamine combined with magnesium sulfate in postoperative analgesia of laparoscopic gynecological surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057759
Enrollment
Unknown
Registered
2022-03-16
Start date
2022-03-11
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

gynecological laparoscopic surgery

Interventions

1:After induction, 0.25mg/kg of esmketamine was injected intravenously, and then 0.15mg/kg/h of esmketamine was continuously injected by pump during operation
2:After induction, 50mg/kg of magnesium sulfate was injected intravenously, and then 8mg/kg/h of magnesium sulfate was continuously injected by pump during operation
3:After induction, 0.15mg/kg esketamine and 25mg/kg of magnesium sulfate was injected intravenously, then 0.075 mg/kg/h esketamine and 4mg/kg/h of magnesium sulfate was continuously injected by pump d
4:After induction,the same amount of normal saline was injected intravenously, and then the same amount of normal saline was continuously injected by pump during operation

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients who intend to undergo gynecological laparoscopic surgery; 2.Age 18-65 years old; 3.BMI 18.5-28 kg/m2 4.ASA grade I~III; 5.The anaesthesia informed consent can be signed.

Exclusion criteria

Exclusion criteria: 1.Patients allergic to narcotic drugs used; 2.Patients with abnormal liver and kidney function before operation; 3.Patients with long-term use of opioids; 4.Patients receiving long-term treatment with calcium channel blockers or magnesium; 5.Patients with atrioventricular conduction disorder; 6.Patients with mental and intellectual abnormalities or inability to communicate normally.

Design outcomes

Primary

MeasureTime frame
VAS;Hydromorphone consumption of PCA;

Secondary

MeasureTime frame
scale scores of QoR-15;scale scores of QoR-15;Postoperative intestinal function recovery time;chronic pain;adverse reactions;Hemodynamic changes;

Countries

China

Contacts

Public ContactAi Yanqiu
Aiyanqiu@163.com13607690334

Outcome results

None listed

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