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Safety and efficacy of sufentanil combined with nalbuphine for postoperative analgesia in elderly patients undergoing laparoscopic radical gastrectomy for gastric cancer

Safety and efficacy of sufentanil combined with nalbuphine for postoperative analgesia in elderly patients undergoing laparoscopic radical gastrectomy for gastric cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114467
Enrollment
Unknown
Registered
2025-12-12
Start date
2025-12-15
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

gastric cancer

Interventions

S1 group:Postoperative analgesic pump formula: 3 µg/kg sufentanil + 16 mg ondansetron + normal saline
S2 group:Postoperative analgesic pump formula: 2.5 µg/kg sufentanil + 2.4 µg/ml dexmedetomidine + 16 mg ondansetron + normal saline
SN group :Postoperative analgesic pump formula: 2 µg/kg sufentanil + 1 mg/kg nalbuphine + 2.4 µg/ml dexmedetomidine + 16 mg ondansetron + saline

Sponsors

Anhui Provincial Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 74 Years

Inclusion criteria

Inclusion criteria: 1. No gender restrictions, aged 60–74 years; 2. BMI: 18.5–24.0 kg/m²; 3. ASA anaesthesia classification II–III; 4. Patient consents to postoperative use of an electronic analgesic pump; 5. Voluntarily signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with known hypersensitivity to nalbuphine hydrochloride or any of its constituents, or with a history of opioid allergy; 2. Use of analgesic sedatives, antiemetics, or antihistamines within 24 hours prior to surgery; 3. Patients with a history of prolonged use of sedative-analgesic medications; 4. Patients anticipated to require admission to the ICU postoperatively; 5. Renal impairment (blood urea nitrogen and/or creatinine > upper limit of normal reference range); hepatic impairment (aspartate aminotransferase and/or alanine aminotransferase > 1.5 times upper limit of normal reference range).

Design outcomes

Primary

MeasureTime frame
Recovery Quality Scale (QoR-15) score ;Adverse reaction rate;

Secondary

MeasureTime frame
Incision and visceral VAS pain scores ;QoR-15 score;Self-rating Anxiety Scale (SAS) scores;Pittsburgh Sleep Quality Index (PSQI) scale score;

Countries

China

Contacts

Public ContactTang Chaoliang

Anhui Provincial Cancer Hospital

chaolt@ustc.edu.cn+86 138 6677 7142

Outcome results

None listed

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