Skip to content

Effect of Biased µ-Opioid Receptor Anesthesia versus Opioid-Free Anesthesia on the Quality of Postoperative Recovery in Patients Undergoing Laparoscopic Cholecystectomy : A Single-Center Randomized Controlled Clinical Trial

Effect of Biased µ-Opioid Receptor Anesthesia versus Opioid-Free Anesthesia on the Quality of Postoperative Recovery in Patients Undergoing Laparoscopic Cholecystectomy : A Single-Center Randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121583
Enrollment
Unknown
Registered
2026-04-01
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

None

Interventions

The Oxalidine group:Anesthesia induction and maintenance using Oliceridine
The no opioid group:Anesthesia induction and maintenance using Esketamine

Sponsors

Shanghai Tongji Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years; 2. ASA I-II; 3. Body mass index 18-30 kg/m^2; 4. Patients scheduled for elective laparoscopic cholecystectomy; 5. Signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. ASA >= III; 2. Heart rate less than 50 beats/min; 3. Left ventricular ejection fraction less than 40%; 4. Sick sinus syndrome or second-degree or higher atrioventricular block; 5. Myocardial infarction; 6. Severe hepatic or renal insufficiency; 7. Allergy or contraindication to drugs that may be used in the trial, or preoperative use of drugs known to have antiemetic effects; 8. Chronic pain (pain persisting or recurring for more than 3 months); 9. Preoperative use of sedatives or analgesics; 10. Mental disorder or inability to communicate; 11. Pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
Quality of Recovery;

Secondary

MeasureTime frame
Postoperative Nausea and Vomiting;Rate of rescue antiemetic use;Severity of PONV;Pain score;Time to emergence;Extubation time;Relevant times (time to first flatus, first defecation, and discharge);Adverse events;

Countries

China

Contacts

Public ContactJianhui Liu

Shanghai Tongji Hospital

jianhuiliu_1246@163.com+86 136 6145 2939

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026