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Clinical study on the improvement of postoperative recovery quality in patients using esketamine assisted general anesthesia technique

Clinical study on the improvement of postoperative recovery quality in patients using esketamine assisted general anesthesia technique

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099548
Enrollment
Unknown
Registered
2025-03-25
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

postoperative recovery quality

Interventions

Control group: C1 group:Conventional propofol total intravenous anesthesia
Experimental group: K1 group:esKetamine intravenous assisted propofol total intravenous anesthesia
Control group:C2 group:Conventional sevoflurane inhalation anesthesia
Experimental group: K2 group:esKetamine assisted sevoflurane inhalation anesthesia
Control group:C3 group:Conventional combined anesthesia of intravenous and inhalation
Experimental group: K3 group:esKetamine intravenous assisted combined anesthesia of intravenous and inhalation

Sponsors

Xuzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: 1.Age between 18-85 years; 2.Elective short-duration laparoscopic surgery with a surgical duration <=2 hours; 3.ASA classification I-III; 4.No communication barriers, clear consciousness; 5.BMI ranging from 18.5-28 kg/m²; 6.Willing to use postoperative intravenous analgesia devices; 7.Ethical compliance, voluntary participation, and signed informed consent.

Exclusion criteria

Exclusion criteria: Exclusion Criteria: 1.Presence of contraindications or allergies to esketamine or other anesthetic drugs; 2.Known or suspected abuse or long-term use of narcotic sedatives or analgesics; 3.Severe hypertension or severe cardiovascular disease; 4.Any cerebrovascular accident within the past 3 months; 5.Pulmonary hypertension, or excessively high intracranial or intraocular pressure; 6.History of mental illness, central nervous system injury, or cognitive dysfunction; 7.Severe hepatic or renal insufficiency; 8.History of use of antidepressants or other psychiatric medications.

Design outcomes

Primary

MeasureTime frame
Recovery quality within 24 hours after surgery;

Secondary

MeasureTime frame
Recovery quality within 48 hours after surgery; Recovery quality within 72 hours after surgery;Quality evaluation of anesthesia recovery in PACU;Changes in EEG of perioperative patients;Monitoring of blood concentration of esketamine;Expression of perioperative inflammation and anti inflammatory marker levels Expression of perioperative inflammation and anti-inflammatory markers levels;postoperative side reactions;

Countries

China

Contacts

Public ContactLiwei Wang

Xuzhou Central Hospital

qiyu1987xiaobao@163.com+86 152 5202 6679

Outcome results

None listed

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