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Oliceridine versus sufentanil hyperalgesia for laparoscopic cholecystectomy: a randomized controlled, double-blind study

Comparison of Oxelidine Versus Sufentanil Advanced Analgesia for Laparoscopic Cholecystectomy: A Randomized Controlled, Double-Blind Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096009
Enrollment
Unknown
Registered
2025-01-16
Start date
2025-02-07
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Pain

Interventions

Ocelidine group (Group O):Ocelidine (0.03mg/kg) is injected when the pneumoperitoneum is stopped at the end of the operation, and the infusion is turned off when the last stitch is given to the surgeo
Sufentanil (Group S):Sufentanil (0.15ug/kg) is injected when the pneumoperitoneum is stopped at the end of the operation, and the infusion is turned off when the surgeon sutures the last stitch.
Placebo group (Group C):At the end of the operation, the same volume of normal saline is injected when the pneumoperitoneum is stopped, and the infusion is closed when the surgeon sutures the last sti

Sponsors

Nanchong Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.·Patients undergoing elective laparoscopic cholecystectomy under general anesthesia; 2.Age:18-65; 3.BMI:19-28kg/m^2; 4.ASA:I-II; 5.All candidates agreed to participate in the study and signed.

Exclusion criteria

Exclusion criteria: 1.Patients with acute heart failure, unstable angina pectoris, severe arrhythmia, poorly controlled hypertension and diabetes, etc; 2.Acute respiratory infections, AE COPD, poorly controlled asthma, etc; 3.ESRD,hepatic dysfunction; 4.Mental disorders include: schizophrenia, mania, bipolar disorder, etc; 5.Allergic to the Oliceridine; 6.Pregnant and lactant women.

Design outcomes

Primary

MeasureTime frame
Pain condition;

Secondary

MeasureTime frame
Postoperative adverse events;Extubation choking reaction;Occurrence of agitation;Time to first postoperative rescue analgesia;Cumulative 24h postoperative rescue analgesic use;

Countries

China

Contacts

Public ContactLi Linji

Nanchong Central Hospital

llj-stephen@163.com+86 155 8300 9555

Outcome results

None listed

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