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Effect of nalbuphine hydrochloride combined with dexmedetomidine on post-operative recovery quality and pain in patients undergoing laparoscopic bariatric surgery

Effect of nalbuphine hydrochloride combined with dexmedetomidine on post-operative recovery quality and pain in patients undergoing laparoscopic bariatric surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074027
Enrollment
Unknown
Registered
2023-07-27
Start date
2023-08-01
Completion date
Unknown
Last updated
2023-07-30

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

Conditions

Metabolic syndrome,bariatric surgery

Interventions

Group ND:Dexmedetomidine (1ug/kg) was pumped 10 minutes before induction, then 0.4ug/kg·h was pumped to 20 minutes before the end of surgery, and then 0.2mg/kg Nalbuphine hydrochloride was administere
Group D:Dexmedetomidine (1ug/kg) was pumped 10 minutes before induction, then 0.4ug/kg·h was pumped to 20 minutes before the end of surgery
Group N:20 minutes before the end of the operation, give 0.2mg/kg Nalbuphine hydrochloride
Group C:Give the same volume of physiological saline

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1, Age:18-65 years old 2,BMI=30kg/m2 3,ASA grade II-III 4,Patients who choose to undergo laparoscopic bariatric surgery

Exclusion criteria

Exclusion criteria: 1,Severe cardiovascular disease, chronic renal failure or liver dysfunction 2,Previous upper abdominal surgery 3,History of serious alcoholism, recent use of opioids, and chronic pain 4,Presence of bradycardia, arrhythmia and hypotension 5,Contraindication of nerve block, such as skin infection at or near the puncture site, coagulation dysfunction 6,Allergies to test drug allergy 7,Long term use of corticosteroid or pregnancy 8,Mental or nervous system disease 9,Refusal to sign informed consent form 10,Participate in other clinical trials at the same time

Design outcomes

Primary

MeasureTime frame
QoR-40;

Secondary

MeasureTime frame
VAS score;Mean artrial pressure;Perioperative use of propofol and remifentanil;Vasoactive drug usage rate;Consumption of remedial analgesics within 24h;Scoring of restlessness during awakening period;Heart rate;Extubation time;Postoperative first time out of bed activity time;First anal exhaust time;Adverse reaction rate;Discharge time;

Countries

China

Contacts

Public ContactWang Guanglei

Department of Anesthesiology, Affiliated Hospital of Xuzhou Medical University

wguanglei2000@163.com+86 138 5208 7156

Outcome results

None listed

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