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Left Celiac Plexus Resection for Pancreatic Cancer at the Body and Tail

A Prospective RCT Study of Distal Pancreatectomy Combined With Left Celiac Plexus Resection for Pancreatic Cancer at the Body and Tail

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02117895
Enrollment
180
Registered
2014-04-21
Start date
2014-01-31
Completion date
2017-01-31
Last updated
2016-08-11

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

Conditions

Pancreatic Cancer

Keywords

Distal Pancreatectomy, Celiac Plexus, Resection, Pancreatic Cancer, Body and Tail

Brief summary

This is a prospective study of left celiac plexus resection for pancreatic cancer at the body and tail during standard distal pancreatectomy.

Detailed description

Pancreatic cancer has a property of nerve invasion. Pancreatic cancer cells first invade the nerves within the pancreas, then reach to the retroperitoneal celiax plexus and ganglion. Previous studies have showed nerve invasion was a negative prognostic factor for pancreatic cancer. Celiac plexus was thought as one the sources of tumor recurrence, which also led to severe abdominal and back pain in pancreatic cancer patients. This study is performed to confirm whether left celiac plexus resection could improve survival and relieve pain of pancreatic cancer patients. Subjects undergoing surgery will be randomized to standard distal pancreatectomy plus left celiac plexus resection versus standard distal pancreatectom. Subjects will be followed every two months for survivorship or death to assess pain, quality of life measures, and narcotic pain control usage. The primary endpoint of overall survival and the secondary endpoint of disease-specific free survival will be determined at two year post surgery.The other pre-specified outcome of pain control will be determined at one year post surgery. Block randomization will be done using a computer generated sheet. All surgeries will be performed under general anesthesia with epidural analgesia. The surgery will be either performed by or under the direct supervision of pancreatic surgeons with experience in pancreas surgery. Operative time, blood loss, blood product replacement and all intraoperative details will be recorded in the proforma. Patients will be shifted postoperatively to the anesthesia care unit (PACU) for observation and subsequently to the recovery or high dependency ward once stabilized. Postoperative details including period of postoperative pancreatic fistula,postoperative haemorrhage,postoperative pancreatitis , hospital stay and other complications will be recorded. Postoperative mortality will be defined as 30-day mortality plus death before discharge after surgery.All collected data will be entered into a statistical software package for subsequent analysis

Interventions

PROCEDURECeliac plexus resection

Celiac plexus at the left side of aorta, between celiac trunk and superior mesenteric artery will be resected.

PROCEDUREPancreatectomy

Standard distal pancreatectomy includes distal pancreatectomy, splenectomy, and regional lymph nodes resection for pancreatic cancer at the body and tail. Regional lymph nodes includes group 8, 10, 11, 18, 7, 9, 14, 15, according to the 2003 edition of lymph nodes group system defined by Japan Pancreas Society (JPS).

Sponsors

Fudan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Signed informed content obtained prior to treatment * Age ≥ 18 years and ≤ 80 years * Eastern Cooperative Oncology Group (ECOG) performance status 0-2 * The pathological staging does not exceed the stage IIB * The expected survival after surgery ≥ 3 months * Tumor locates at the body and tail of the pancreas without distant metastasis * No celiac trunk and superior mesenteric artery invasion by Loyer grading * No operation contraindication

Exclusion criteria

* The pathological staging exceed the stage IIB * Pancreatic cancer at the head of the pancreas * Benign tumor at the body and tail of the pancreas * Distant metastasis * Severe important organ function impairment * Active second primary malignancy or history of second primary malignancy within the last 3 years * Pregnant or nursing women * Human immunodeficiency virus (HIV)-positive patients * Patients who are unwilling or unable to comply with study procedures

Design outcomes

Primary

MeasureTime frame
Overall survival2 years

Secondary

MeasureTime frame
Disease-specific, recurrence-free survival2 years

Other

MeasureTime frameDescription
Pain Control12 monthsPaint control will be assess by the Visual Analogue Scale (VAS)

Countries

China

Contacts

Primary ContactXian-Jun Yu, M.D.,Ph.D
yuxianjun88@hotmail.com+86 21 64175590

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026