跳至主要内容
临床试验/NCT03752086
NCT03752086Unknown不适用

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

Tongji Hospital1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2019年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
200
试验地点
1
主要终点
pancreatic fistula

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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.

排除标准

  • •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.

研究组 & 干预措施

Greater omentum binding

Experimental

Bind greater omentum to pancreatic stump after distal pancreatectomy

干预措施: greater omentum binding (Procedure)

Pancreatic stump exposed

Experimental

pancreatic stump exposed without binding greater omentum after distal pancreatectomy

干预措施: Pancreatic stump exposed without omentum binding (Procedure)

结局指标

主要结局

pancreatic fistula

时间窗: 90 days

Incidence of pancreatic fistula defined by ISGPF classification

次要结局

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

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Renyi Qin

Professor, Chief physician

Tongji Hospital

研究点 (1)

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