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NCT07148830Recruiting

Mesopancreatic Excision for Pancreatic Duct Adenocarcinoma.

Effect of Mesopancreatic Excision for Pancreatic Duct Adenocarcinoma on Local Disease Control and Survival.

Source: ClinicalTrials.gov · Last updated 11 Sept 2026

Brief summary (registry, in English)

Pancreatic ductal adenocarcinoma (PDAC) is an aggressive cancer with high rates of local recurrence and distant metastasis. Recent evidence suggests that mesopancreatic excision (TMpE) may improve R0 resection rates, reduce local recurrence, and enhance overall survival compared to standard pancreatoduodenectomy. However, most existing studies are retrospective with heterogeneous patient populations and surgical techniques. This prospective study aims to evaluate the impact of mesopancreatic excision, a surgical technique involving the meticulous removal of retroperitoneal tissue surrounding major peripancreatic vessels, on local disease control and overall survival in patients undergoing pancreaticoduodenectomy for resectable PDAC. The study will also assess R0 resection rates, disease-free survival, recurrence patterns and perioperative outcomes.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
100 (estimated)
First submitted
17 Aug 2025
Start date
1 Apr 2024
Primary completion date
1 Apr 2027
Lead sponsor
Minia University
NCT number
NCT07148830

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From 1 Apr 2024 to the primary completion date, 1 Apr 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior neoadjuvant chemotherapy or radiotherapy (to isolate TMpE effect; may be amended for subgroups).
  • Patients who have received prior radiotherapy to the abdomen.

Other illness

  • Active second malignancy.
  • Severe comorbidities precluding surgery (e.g., uncontrolled cardiac disease).

Other

  • Borderline resectable or unresectable PDAC.
  • Distant metastases.
  • Periampullary tumors other than pancreatic adenocarcinoma
  • Pregnancy or lactation.
  • Patients unwilling or unable to provide informed consent.

Who the study is looking for

  • Age ≥18 years.
  • Patients scheduled to undergo pancreaticoduodenectomy with planned mesopancreatic excision.
  • Histologically confirmed PDAC of the pancreatic head (via endoscopic ultrasound-guided biopsy).
  • Resectable disease per National Comprehensive Cancer Network(NCCN) guidelines (no distant metastases, no arterial involvement \>180°, venous involvement reconstructable).
  • Eastern Cooperative Oncology Group(ECOG) performance status 0-2.
  • Adequate organ function (e.g., bilirubin \<1.5x upper limit of normal(ULN), creatinine clearance \>50 mL/min).
  • Informed consent.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Liver and GIT hospital , Minia University
Coordinator of this site? Confirm its status
MinyaEgyptRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.