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The analgesic effect of tegileridine in elderly patients after laparoscopic abdominal tumor surgery: a randomized controlled trial

The analgesic effect of tegileridine in elderly patients after laparoscopic abdominal tumor surgery: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110485
Enrollment
Unknown
Registered
2025-10-14
Start date
2025-10-15
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Postoperative pain

Interventions

Morphine Group:Postoperative analgesia was administered via a patient-controlled intravenous analgesia (PCIA) regimen. A 0.9% sodium chloride solution (45 mL) served as the diluent for morphine (1 mL:
Tegileridine Group:Postoperative analgesia was administered via a patient-controlled intravenous analgesia (PCIA) regimen. A 0.9% sodium chloride solution (45 mL) served as the diluent for tegileridin

Sponsors

Zhengzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: Age >>= 65 years, ASA 2-3 classification, BMI 18.5-30 kg/m^2, elective laparoscopic abdominal tumour surgery (hepatobiliary, gastrointestinal)

Exclusion criteria

Exclusion criteria: Severe cardiac insufficiency (NYHA Class III-IV), severe hepatic dysfunction (Child-Pugh Class C), renal impairment (undergoing dialysis preoperatively), pregnancy or lactation, history of allergy to study medication, chronic pain or preoperative analgesic use, administration of medications potentially affecting analgesic response (anticonvulsants, antidepressants or antipsychotics), psychiatric or neurological disorders.

Design outcomes

Primary

MeasureTime frame
Incidence of moderate to severe pain during physical activity within 24 hours post-surgery (moderate to severe pain defined as NRS pain score >=4);

Secondary

MeasureTime frame
Incidence of moderate to severe pain at rest within 24 hours post-surgery;Rate of rescue analgesia within 24 hours post-surgery;Number of PCIA compressions within 24 hours post-surgery;Pain satisfaction score at 24 hours post-surgery (assessed using the NRS scale, 0–10 points, where a higher score indicates greater satisfaction);Time of first ambulation;time to first flatus;

Countries

China

Contacts

Public ContactGuanyu Yang

Zhengzhou Central Hospital

anesygy@qq.com+86 157 3831 4002

Outcome results

None listed

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