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Clinical Trials/NCT03752086
NCT03752086UnknownNot Applicable

Intra-operative Greater Omentum Binding to the Pancreatic Stump to Prevent Post-operative Pancreatic Fistula Following Distal Pancreatectomy: A Randomized Clinical Trial

Tongji Hospital1 site in 1 country200 target enrollmentStarted: January 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
200
Locations
1
Primary Endpoint
pancreatic fistula

Study Overview

Brief Summary

Background and aim: Distal pancreatectomy (DP) is often performed for primary benign or malignant lesions occurred in the body or tail of the pancreas. The occurrence of pancreatic fistula (PF) after DP remains high, ranging from 5% to 60%, despite in high-volume centers. Management of pancreatic stump to prevent PF has been a long-standing issue in pancreatic surgery. Our group has proposed greater omentum binding as a novel approach to secure pancreatic stump with the purpose of reducing PF. With respect to the previous preliminary data which demonstrated greater omentum binding of pancreatic stump significantly reduced the occurrence of PF based on a small prospective cohort, we therefore aimed to verify the safety and effectiveness of this novel approach in a large prospective randomized cohort.

Method: TJBDPS06 is a prospective, randomized controlled, parallel-group, superiority trial in a single high-volume pancreatic center. A total of 200 patients who will receive DP and fulfill the inclusion criteria will be randomly allocated to the greater omentum binding group or the group without this step in an enhanced recovery after surgery (ERAS) setting. The trial hypothesize that greater omentum binding of pancreatic stump could safely and effectively secure pancreatic stump following DP, therefore reducing the occurrence of PF. The primary outcome is PF within 90 days after DP. The secondary outcomes are overall morbidly, mortality, and major complications (Clavien-Dindo ≥III) within 90 days following DP. The duration of entire trial is presumably three years, including prearrangement, two-year inclusion period, and data analysis.

Discussion: The current trial will be the first in demonstrating safety and effectiveness of greater omentum binding of pancreatic stump following DP in a large high-volume pancreatic center. This approach will offer an inexpensive, technically easy, and secure coverage technique for the pancreatic stump in DP and may be particularly useful for patients with a soft pancreas which is a markedly risk factor of PF.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All patients who undergo DP whether made by open or laparoscopic surgery;
  • Patients age 18 to 75 years;
  • Patients benefit from distal pancreatectomy according to NCCN guidelines;
  • The subject understands the nature of this trial and willing to comply, and ability to provide written informed consent.

Exclusion Criteria

  • Distant metastases: peritoneal carcinomatosis, liver metastases, distant lymph node metastases, involvement of other organs;
  • History of abdominal disease or surgery which may results in obvious omentum adhesion;
  • Synchronous malignancy in other organs;
  • Patients with high operative risk as defined by the American Society of Anesthesiologists (ASA) score >4;
  • Pregnant women.

Arms & Interventions

Greater omentum binding

Experimental

Bind greater omentum to pancreatic stump after distal pancreatectomy

Intervention: greater omentum binding (Procedure)

Pancreatic stump exposed

Experimental

pancreatic stump exposed without binding greater omentum after distal pancreatectomy

Intervention: Pancreatic stump exposed without omentum binding (Procedure)

Outcomes

Primary Outcomes

pancreatic fistula

Time Frame: 90 days

Incidence of pancreatic fistula defined by ISGPF classification

Secondary Outcomes

  • mortality(90 days)
  • major complications (Clavien-Dindo ≥III)(90 days)
  • overall morbidity(90 days)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Renyi Qin

Professor, Chief physician

Tongji Hospital

Study Sites (1)

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