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Effect of Intravenous Infusion of Esketamine on Recovery Outcome Variables and the Quality of Postoperative Recovery in Patients Undergoing Laparoscopic Bariatric Surgery

Effect of Intravenous Infusion of Esketamine on Recovery Outcome Variables and the Quality of Postoperative Recovery in Patients Undergoing Laparoscopic Bariatric Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066138
Enrollment
Unknown
Registered
2022-11-25
Start date
2022-11-30
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Bariatric Surgeries

Interventions

Esketamine group:Esketamine infusion: 0.5mg/kg/h
control group:Pump saline pump injection

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. American Society of Anesthesiologists (ASA) physical status II–III; 2. Age between 18 and 65 years; 3. BMI >= 30 kg/m^2; 4. Planned to undergo laparoscopic bariatric surgery prior to registration.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of allergy to any drug used in the study; 2. Previous history of hyperthyroidism and pheochromocytoma, severe cardio-cerebrovascular disease,hypertension grade III (very high risk), severe arrhythmias, or hemodynamic instability; 3. Severe hepatorenal insufficiency ; 4. Recent use of any tricyclic antidepressants, monoamine oxidase inhibitors, sedative, opioid, or sleep-inducing drugs in the past month; 5. Anemia (Hb < 9.0 mg/dl); 6. Unable to cooperate with the researcher for any reason; 7. Hearing or a visual impairment, speech comprehension impairment, mental illness; 8. Refusal to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Quality of postoperative recovery;

Secondary

MeasureTime frame
Time to extubation;Time to eye opening;Time to spontaneous breathing;postoperation pain;sleep quality;length of hospital stay;time of PACU stay;CNS adverse events(Hallucinations/Vivid dreams/Confusion and disorientation/Visual disturbances);Utilization rate of vasoactive drugs;PONV;postoperative activity time;Postoperative urinary retention;dose of Intra-operative propofol used;dose of Intra-operative remifentanil used;Postoperative analgesic drug dosage;hyoxemia;Qor-40;

Countries

China

Contacts

Public ContactZhiping Wang

Affiliated Hospital of Xuzhou Medical University

121319811@qq.com+86 151 6202 5028

Outcome results

None listed

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