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A Study of a Novel Analgesic Protocol on Optimizing the Quality of Recovery After Gallbladder Surgery in Women

Optimization of Ocelidine Combined with Transverse Fascial Block on Quality of Recovery After Laparoscopic Gallbladder Surgery in Women: A Single-center Randomized Controlled Study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600129411
Enrollment
Unknown
Registered
2026-08-04
Start date
2025-12-01
Completion date
Unknown
Last updated
2026-08-10

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

Conditions

Patients with gallbladder diseases requiring laparoscopic cholecystectomy

Interventions

Oliceridine Group:Oliceridine Combined with Transversus Abdominis Plane Block for Multimodal Analgesia
Sufentanil Group:Sufentanil Combined with Transversus Abdominis Plane Block for Multimodal Analgesia

Sponsors

Shaanxi 215 Hospital of nuclear industry
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Female, age 18-64 years; 2. American Society of Anesthesiologists (ASA) grades I to III; 3. Planned to undergo elective laparoscopic cholecystectomy; 4. Postoperative nausea and vomiting (PONV) risk score (Apfel score) >= 2 points (including at least two items "female" and "non-smoker").

Exclusion criteria

Exclusion criteria: 1. Long-term or regular use of opioid analgesics or antiemetic drugs. 2. Known allergy to local anesthetics (e.g., ropivacaine), or contraindications to transversus abdominis plane block (e.g., infection at puncture site, coagulation dysfunction). 3. Pregnant or lactating women. 4. Severe hepatic or renal insufficiency (e.g., Child-Pugh class C, or estimated glomerular filtration rate eGFR < 30 mL/min/1.73m²). 5. History of severe neurological or psychiatric disorders that may interfere with the assessment of pain or nausea. 6. Inability to comprehend the study content or refusal to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Outcome:Postoperative quality recovery score (QoR-15) at 24 hours postoperatively;

Secondary

MeasureTime frame
Time to first get out of bed after surgery;Incidence and severity of postoperative nausea and vomiting (PONV);Total dose of remifentanil during the operation;Postoperative VAS pain score at rest and on coughing;Outcome:Rate of rescue antiemetic use;Incidence of postoperative adverse events;Preoperative and 48 hours postoperative quality recovery score (QoR-15);Postoperative length of hospital stay;

Countries

China

Contacts

Public ContactChen Peng

Shaanxi 215 Hospital of nuclear industry

ws-cp@163.com+86 29 3208 8351

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026