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A Prospective Randomized Controled Trial of Postoperative Thoracic Epidural Analgesia Versus Intravenous Patient-controlled Analgesia After laparoscopic pancreaticoduodenectomy

A Prospective Randomized Controled Trial of Postoperative Thoracic Epidural Analgesia Versus Intravenous Patient-controlled Analgesia After laparoscopic pancreaticoduodenectomy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015948
Enrollment
Unknown
Registered
2020-05-02
Start date
2018-05-01
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Analgesia after laparoscopic pancreatoduodenectomy

Interventions

experimental group:Thoracic Epidural Analgesia
control group:Intravenous Patient-controlled Analgesia
experimental group:ERAS protocol (Study Protocol)
control group:Conventional care (Study Protocol)

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Eligible patients were between 18 years and 75 years undergoing selective pancreaticoduodenectomy for ampullar periampullary or pancreatic head benign and malignant lesions; 2. Laparoscopic pancreaticoduodenectomy were successful performed; 3. The coagulation function is normal, platelet count 80-350 x 10^9/L 4. The renal function is normal.

Exclusion criteria

Exclusion criteria: 1. Laparoscopic pancreaticoduodenectomy convert open surgery,anticoagulation was needed when major vascular resection was performed intraoperatively; 2. The coagulation function is abnormal,epidural placement should be avoided during Low molecular weight heparin therapy or 24 hours after Low molecular weight heparin therapy; 3. Spine malformation,traumatic history of spine,psychiatric condition or communication (language) barriers should be precluded; 4. Patients with fever,evidence of infection,chronic pain,long-term narcotic use,history of anaphylaxis to local anesthetics or narcotics or surgery in the previous 30 days under general anesthesia.

Design outcomes

Primary

MeasureTime frame
postoperative pain score;Total opioid consumption;

Secondary

MeasureTime frame
Time of intestinal function recovery;side effects of different analgesic methods;length of postoperative hospital stay;postoperative morbidity;Perioperative renal function;

Countries

China

Contacts

Public ContactPeng Bing

West China Hospital, Sichuan University

pengbing84@hotmail.com+86 18980601481

Outcome results

None listed

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