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A Trial of Early Percutaneous Catheter Drainage of Sterile Pancreatic Fluid Collections in Severe Acute Pancreatitis (EPCDSAP)

Primary Purpose

Severe Acute Pancreatitis

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Puncture and drainage
Sponsored by
Second Affiliated Hospital, School of Medicine, Zhejiang University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Severe Acute Pancreatitis focused on measuring severe acute pancreatitis, sterile acute peripancreatic fluid collections, percutaneous catheter drainage

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age of 18 years to 70 years; and
  2. Pain characteristic of pancreatitis; and
  3. Elevated serum lipase or amylase (≥3-fold upper normal range); and
  4. Persistent organ failure >48 hours; and
  5. Organ dysfunction occurred within 7 days after onset of pain; and
  6. Presentation with a width of ≥2cm of APFCs in the peripheral tissues of the pancreas, the cyst of lesser omentum , or the paracolic sulci on CT image.

Exclusion Criteria:

  1. History diseases of chronic organ dysfunction; or
  2. Traumatic pancreatitis; or
  3. Post-endoscopic retrograde cholangiopancreatography(ERCP) pancreatitis; or
  4. Severe coagulopathy (INR>2); or
  5. Severe thrombocytopenia (PLT≤50×109/L); or
  6. No suitable route for puncturing; or
  7. Pregnancy; or
  8. Absent of informed consent from patient or representative.

Sites / Locations

  • The second affiliated hospital of Zhejiang UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Puncture and Drainage

Conservative therapy

Arm Description

The enrolled SAP patients are administered puncture and drainage use 8-F or 10-F pigtail tube under guidance of B ultrasound or CT scan.

The enrolled SAP patients are administered conservative therapy and without puncture and prolonged drainage.

Outcomes

Primary Outcome Measures

Mortality
Determine and compare the death rates in patients who are administered drainage and conservative therapy: Assess the total number of cases of death in each group (Treatment and control)

Secondary Outcome Measures

Secondary infection of peripancreatic collections
Compare the secondary infection rates of peripancreatic collections in patients who are administered drainage and conservative therapy: Assess the total numbers of cases of secondary infection of peripancreatic collections in each group (Treatment and control)
New set of organ failure
Compare the new set of organ failure rates in patients who are administered drainage and conservative therapy: Assess the total numbers of cases of new set of organ failure in each group (Treatment and control)
Length of hospital/ICU stay
Compare the length of hospital/ICU stay in patients who are administered drainage and conservative therapy
Aggressive procedures: open necrosectomy and minimally invasive retroperitoneal necrosectomy
Compare the aggressive procedures rates in patients who are administered drainage and conservative therapy.
Abdominal hemorrhage
Compare the abdominal hemorrhage rates in patients who are administered drainage and conservative therapy.
Digestive tract fistula
Compare the digestive tract fistula rates in patients who are administered drainage and conservative therapy.

Full Information

First Posted
May 30, 2017
Last Updated
October 5, 2017
Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
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1. Study Identification

Unique Protocol Identification Number
NCT03185806
Brief Title
A Trial of Early Percutaneous Catheter Drainage of Sterile Pancreatic Fluid Collections in Severe Acute Pancreatitis
Acronym
EPCDSAP
Official Title
A Randomized, Multicenter and Prospective Trial of Early Percutaneous Catheter Drainage of Sterile Pancreatic Fluid Collections in Severe Acute Pancreatitis
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Unknown status
Study Start Date
October 6, 2017 (Anticipated)
Primary Completion Date
October 6, 2020 (Anticipated)
Study Completion Date
October 6, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The acute peripancreatic fluid collections (AFPCs) is the most common complication in severe acute pancreatitis (SAP). There are controversies on optimal timing for drainage of APFCs in SAP. The early-stage percutaneous catheter drainage (PCD) of sterile peripancreatic fluid collections is questioned as a result of the major cause of secondary infection. The aim of the present randomized controlled trial is to compare the outcomes in terms of mortality, secondary infection of peripancreatic collections, organ failure, length of hospital/ICU stay and inflammatory biomarkers between the early-stage PCD of sterile AFPCs and conservative therapy.
Detailed Description
The AFPCs is the most common complication in SAP and debate continues regarding the appropriate timing for drainage of sterile APFCs in SAP patients. Some researchers have reported that the massive amounts of inflammatory mediators in the peripancreatic fluid may aggravate the inflammatory reaction and contribute to organ failure (OF) when liberated into the bloodstream by peritoneal absorption. Additionally, bacterial colonization of APFCs may lead to peritoneal abscess formation and sepsis. In a recent study, Wang et al. revealed that early-stage PCD effectively attenuated the peritoneal pressure and decreased the incidence of infection and OF. Finally, APFCs and secondary infection are considered major causes of alimentary tract hemorrhage. Based on these factors, prompt drainage of APFCs seems reasonable for patients in early SAP. In addition, unlike the original 1992 Atlanta classification guidelines (1992-AC), the revision of the 1992-AC by international consensus in 2012 (2012-RAC) highlighted the significance of persistent OF in the classification of SAP. To be exact, those patients diagnosed with SAP according to the 1992-AC without OF or with transient OF were reclassified as having mild AP (MAP) or moderate severity AP (MSAP) by the 2012-RAC. Therefore, many studies have reported changes in the treatment of SAP in the early stages since the 2012-RAC were published. We have retrospectively analyzed 361 patients with AP and found that the early-stage PCD of sterile APFCs in SAP-2012RAC patients can significantly reduce the mortality rate. However, on the contrary, the mainstream viewpoint holds that drainage is not necessary in the absence of infection of the peripancreatic fluid as the fluid can be absorbed completely and sterile PCD may increase the risk of iatrogenic infection. However, these mainstream views aimed at 1992-AC's SAP patients, which actually contain 2012-RAC's SAP and MSAP. Therefore, we hypothesized that the introduction of new AP severity classification methods may alter the indications for early aseptic drainage of AFPCs. Does early PCD of sterile APFCs benefits patients or increases the secondary infection rate? In view of these problems, we plan to design a randomized controlled trial to compare the outcomes in terms of mortality, secondary infection of peripancreatic collections, organ failure, length of hospital/ICU stay and inflammatory biomarkers between the early-stage PCD of sterile AFPCs and conservative therapy. The aim of this prospective study is to investigate whether early PCD of sterile AFPCs can be used to SAP patients with AFPCs at early stage.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Acute Pancreatitis
Keywords
severe acute pancreatitis, sterile acute peripancreatic fluid collections, percutaneous catheter drainage

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Puncture and Drainage
Arm Type
Experimental
Arm Description
The enrolled SAP patients are administered puncture and drainage use 8-F or 10-F pigtail tube under guidance of B ultrasound or CT scan.
Arm Title
Conservative therapy
Arm Type
No Intervention
Arm Description
The enrolled SAP patients are administered conservative therapy and without puncture and prolonged drainage.
Intervention Type
Device
Intervention Name(s)
Puncture and drainage
Intervention Description
The enrolled SAP patients are punctured under guidance of B ultrasound or CT scan, and prolonged drained by 8-F or 10-F pigtail tube
Primary Outcome Measure Information:
Title
Mortality
Description
Determine and compare the death rates in patients who are administered drainage and conservative therapy: Assess the total number of cases of death in each group (Treatment and control)
Time Frame
From date of admisstion until the date of in-hospital death or death within two weeks after discharging, whichever came first, assessed up to 1 year.
Secondary Outcome Measure Information:
Title
Secondary infection of peripancreatic collections
Description
Compare the secondary infection rates of peripancreatic collections in patients who are administered drainage and conservative therapy: Assess the total numbers of cases of secondary infection of peripancreatic collections in each group (Treatment and control)
Time Frame
From date of admisstion until the secondary infection of peripancreatic collections occurred, assessed up to 100 days
Title
New set of organ failure
Description
Compare the new set of organ failure rates in patients who are administered drainage and conservative therapy: Assess the total numbers of cases of new set of organ failure in each group (Treatment and control)
Time Frame
From date of admisstion until new set of organ failure occurred, assessed up to 100 days
Title
Length of hospital/ICU stay
Description
Compare the length of hospital/ICU stay in patients who are administered drainage and conservative therapy
Time Frame
From date of admisstion until the patient is transfered to normal ward or discharge, whichever came first, assessed up to 1 year.
Title
Aggressive procedures: open necrosectomy and minimally invasive retroperitoneal necrosectomy
Description
Compare the aggressive procedures rates in patients who are administered drainage and conservative therapy.
Time Frame
From date of admisstion until the patient receives aggressive procedures, assessed up to 100 days
Title
Abdominal hemorrhage
Description
Compare the abdominal hemorrhage rates in patients who are administered drainage and conservative therapy.
Time Frame
From date of admisstion until the abdominal hemorrhage occurred, assessed up to 100 days
Title
Digestive tract fistula
Description
Compare the digestive tract fistula rates in patients who are administered drainage and conservative therapy.
Time Frame
From date of admisstion until the Digestive tract fistula occurred, assessed up to 100 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age of 18 years to 70 years; and Pain characteristic of pancreatitis; and Elevated serum lipase or amylase (≥3-fold upper normal range); and Persistent organ failure >48 hours; and Organ dysfunction occurred within 7 days after onset of pain; and Presentation with a width of ≥2cm of APFCs in the peripheral tissues of the pancreas, the cyst of lesser omentum , or the paracolic sulci on CT image. Exclusion Criteria: History diseases of chronic organ dysfunction; or Traumatic pancreatitis; or Post-endoscopic retrograde cholangiopancreatography(ERCP) pancreatitis; or Severe coagulopathy (INR>2); or Severe thrombocytopenia (PLT≤50×109/L); or No suitable route for puncturing; or Pregnancy; or Absent of informed consent from patient or representative.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tingbo Liang, MD,PhD
Phone
86-571-87315006
Email
liangtingbo@zj.edu.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Yun Zhang, MD
Phone
86-571-87315006
Email
bigzyun@hotmail.com
Facility Information:
Facility Name
The second affiliated hospital of Zhejiang University
City
Hangzhou
State/Province
Zhejiang
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yun Zhang, MD

12. IPD Sharing Statement

Learn more about this trial

A Trial of Early Percutaneous Catheter Drainage of Sterile Pancreatic Fluid Collections in Severe Acute Pancreatitis

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