Safety and Efficacy of Anricfen for Postoperative Analgesia and Rehabilitation Promotion After Pancreaticoduodenectomy.Intervention Measures: For Normal Adults, Administer Ariceptin Injection Intravenously Post-operation at a Dose of 1 μg/Kgevery 8 Hours for Three Consecutive Days After Surgery.

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-80
SponsorThe Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

About this trial

Exploring the effectiveness and safety of early use of Ariceptinfen after pancreaticoduodenectomy in alleviating postoperative pain and promoting recovery of patients.

Main objective: To explore the analgesic effect of Anricfen after pancreaticoduodenectomy.

Secondary objective: To explore the impact of Anricfen on the accelerated recovery after pancreaticoduodenectomy.

Exploratory objective: To investigate the biomarkers of Anricfen's analgesic effect after pancreaticoduodenectomy, as well as its correlation factors with tumor pathology.

Eligibility criteria

Qualifiers

Patients who underwent pancreatic surgery, including pancreaticoduodenectomy (PD), pancreatic-preserving pancreaticoduodenectomy (PPPD), and laparoscopic pancreaticoduodenectomy (LPD)

Age ≥ 18 years old and < 80 years old

ASA Ⅰ-Ⅲ

Be able to clearly understand and voluntarily participate in the research

Disqualifiers

Merging severe primary diseases involving the heart, brain, liver, kidneys and hematopoietic system

History of long-term use of psychotropic drugs and cognitive dysfunction

Having a history of acute poisoning from alcohol, sleeping pills, painkillers or other drugs that affect the central nervous system

Pregnancy or lactation period

Trial design

Treatments tested in this trial

  • Experimental Group
  • Anrikefon

Treatment groups

35 Participants
are divided into 1 treatment group