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Pancreatic Fistula After Minimally Invasive Enucleation

Factors Influencing the Occurrence of Pancreatic Fistula After Minimally Invasive Pancreatic Enucleation and Predictive Models: a Prospective Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06557408
Enrollment
173
Registered
2024-08-16
Start date
2019-07-01
Completion date
2024-07-30
Last updated
2024-11-07

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

Conditions

Pancreatic Neuroendocrine Tumor, Pancreatic Tumor, Benign, Solid Pseudopapillary Tumor of the Pancreas

Keywords

Pancreatic benign or low-grade malignant tumors, Minimally invasive enucleation, Postoperative pancreatic fistula, Prediction model

Brief summary

Patients suffering from postoperative pancreatic fistula (POPF) after minimally invasive enucleation (MIEN) show a characteristic pattern of longer duration and milder symptoms, which is different from pancreatic fistula after standard pancreatectomy. This study aimed to analyze the factors influencing clinically-relevant POPF (CR-POPF) after MIEN, investigate and develop a personalized predictive model for accurate prediction of CR-POPF.

Detailed description

Minimally invasive enucleation (MIEN) has been widely used in managing benign and low-grade malignant pancreatic tumors, showing better protection of pancreatic function and better long-term outcomes compared to standard pancreatectomy. However, the incidence of postoperative pancreatic fistula (POPF) after MIEN is higher compared to standard resection, mainly since a large part of the pancreatic wound is exposed, and the main pancreatic duct may be exposed or injured, etc. POPF is the most important postoperative complication, and it has become a major constraint to the conduct of pancreatic MIEN. Although risk factors and predictive models for POPF in standard pancreatic surgery have been reported in the past, no predictive models have been reported specifically for MEN. With the increasing adoption of MIEN, there is an urgent need for a predictive model to guide the treatment and prognosis of POPF. Therefore, this study aims to conduct a cohort study, with data prospectively collected and retrospectively analyzed. The result of this study will provide a valuable reference for the development and application of MIEN.

Interventions

None listed

Sponsors

Fudan University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. Age between 18 and 70 years, regardless of gender. 2. Benign or low-grade malignant tumor of the pancreas. 3. Patients evaluated according to guidelines that indicate a need for surgery or a strong request for surgery. 4. Feasibility of performing minimally invasive pancreatic tumor enucleation based on preoperative imaging evaluation. 5. Patients with an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. 6. Willingness to comply with the follow-up programme of the study and other protocol requirements. 7. Voluntary participation and signed informed consent.

Exclusion criteria

1. Concurrent presence of other malignant tumors. 2. Intraoperative frozen pathology or postoperative pathology indicating the tumor to be malignant, requiring oncological resection instead. 3. Severe impairment of cardiac, hepatic, or renal function (e.g., NYHA class 3-4 heart failure, ALT and/or AST levels exceeding three times the upper limit of normal, creatinine levels exceeding the upper limit of normal). 4. Missing data due to patient loss of followup, etc.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of Clinically Relevant Postoperative Pancreatic FistulaWithin 90 days after surgery.Clinically Relevant Pancreatic Fistula including Grade B fistulas, which require treatment beyond simple drainage, as well as Grade C fistulas.

Secondary

MeasureTime frameDescription
Perioperative complication rate according to the Clavien-Dindo classificationWithin 90 days after surgery.Adverse events occurring during or after surgery reported according to the Clavien-Dindo classification.

Countries

China

Outcome results

None listed

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