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Effect of different analgesic drugs on perioperative and postoperative pain after laparoscopic cholecystectomy: a prospective study

Effect of different analgesic drugs on perioperative and postoperative pain after laparoscopic cholecystectomy: a prospective study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078853
Enrollment
Unknown
Registered
2023-12-20
Start date
2023-12-25
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

gallbladder and biliary diseases

Interventions

Nalbuphine group:intravenous nalbuphine before anesthesia induction
Tramadol group:intravenous tramadol before anesthesia induction
Butorphanol tartrate group:intravenous Butorphanol tartrate before anesthesia induction
Flurbiprofen group:intravenous Flurbiprofen before anesthesia induction
Sufentanil group:intravenous Sufentanil before anesthesia induction

Sponsors

Huishan District People's Hospital of Wuxi
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: All the patients included in this review underwent elective laparoscopic cholecystectomy. 1.male and female patients between 18 and 65 years of age; 2.American Society of Anesthesiology (ASA) score of I or II ; 3.body mass index (BMI) of 18–30 kg/m2;

Exclusion criteria

Exclusion criteria: 1.unplanned emergency surgery; 2.severe cardiac insufficiency(EF < 30%) or serious lung diseases( type I or II respiratory failure); 3.mental illness or diminished cognitive function, or taking long-term antipsychoticor related drugs, or drug users; 4.allergies or contraindications to any of the study drugs; 5.Patients who had contraindications to nerve block, and can-not tolerate a phrenic nerve block. 6. long-standing pain or neuropathic pain; 7.gallstones with gallbladder perforation, diffuse peritonitis or acute pyogenic cholangitis; 8.illiterate, or understand the study scoring.

Design outcomes

Primary

MeasureTime frame
Pain conditions, including incision pain, visceral pain, opioid-induced hyperalgesia, and referred pain (shoulder pain).;

Secondary

MeasureTime frame
General characteristics of the patients,Demographic and clinical characteristics;the perioperative conditions;Postoperative Situation and the wake-up period conditions;adverse reactions;

Countries

China

Contacts

Public ContactLiu Man

Huishan District People's Hospital of Wuxi

liuman9666@163.com+86 182 6190 5897

Outcome results

None listed

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