Timing of Transmural Stent Removal in Necrotizing Pancreatitis (TTSRNP)
Primary Purpose
Acute Pancreatitis, Necrotizing Pancreatitis, Walled-Off Necrosis
Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Stent removed by the novel strategy
Stent removed by the conventional strategy
Sponsored by
About this trial
This is an interventional treatment trial for Acute Pancreatitis focused on measuring Necrotizing pancreatitis, Endoscopic transmural necrosectomy, Lumen-apposing metal stent
Eligibility Criteria
Inclusion Criteria:
- Patients diagnosed with necrotizing pancreatitis according to the 2012 Atlanta classification criteria;
- Patients aged between 18 and 65 years;
- Patients who signed the informed consent;
Exclusion Criteria:
- Patients without transmural stent placement;
- Patients with transmural plastic stent not metal stent placement before enrollment;
- Patients who underwent endoscopic transmural necrosectomy in other hospitals before admission;
- Patients complicated with chronic pancreatitis;
- Patients complicated with pancreatic tumor;
- Pregnant or lactating women.
Sites / Locations
- The First Affiliated Hospital of Nanchang University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
The novel strategy group
The conventional strategy group
Arm Description
The stents were removed during the last necrosectomy when the endpoint of necrosectomy was achieved
The stent was removed after the last necrosectomy when clinical symptoms were relieved and fluid was nearly completely resolved confirmed by CT image
Outcomes
Primary Outcome Measures
The incidence of composite complications
The composite complications included new-onset organ failure or systemic complications、new-onset infectious pancreatic necrosis、abdominal or gastrointestinal bleeding, intestinal fistula, stent occlusion and stent migration.
Secondary Outcome Measures
The incidence of technical success
Technical success was defined by stent removed successfully.
The incidence of clinical success
Clinical success was defined as nearly completely resolution or <2 cm of collection assessed by image at the three-month follow-up without additional open surgery or death.
The number of endoscopic transmural necrosectomy sessions
Total sessions of patients undergoing endoscopic transmural necrosectomy.
The number of additional endoscopic transmural necrosectomy sessions after stent removal
Additional sessions of patients undergoing endoscopic transmural necrosectomy. after stent removal.
Length of stent placement
The duration time from stent placement to stent removal.
The incidence of open surgery
The incidence of patients needing open surgery after minimally invasive treatment.
All-cause mortality
The mortality whatever the cause is.
Length of hospital stay
The length of hospital stay due to necrotizing pancreatitis.
The incidence of readmission
The incidence of readmission after index discharge due to pancreatitis related problems.
The hospital cost
The hospital cost during hospitalization.
Full Information
NCT ID
NCT04963868
First Posted
June 21, 2021
Last Updated
July 6, 2021
Sponsor
The First Affiliated Hospital of Nanchang University
1. Study Identification
Unique Protocol Identification Number
NCT04963868
Brief Title
Timing of Transmural Stent Removal in Necrotizing Pancreatitis
Acronym
TTSRNP
Official Title
Timing of Transmural Stent Removal in Necrotizing Pancreatitis Undergoing Endoscopic Transmural Necrosectomy: A Randomized Controlled Study
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 1, 2022 (Anticipated)
Primary Completion Date
June 1, 2024 (Anticipated)
Study Completion Date
December 1, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The First Affiliated Hospital of Nanchang 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
Although metal stents have been widely used in the endoscopic step-up approach for necrotizing pancreatitis, the exact timing of transmural stent removal has not been well studied. In this prospective, open-label, randomized controlled study, we recruited and enrolled consecutive patients with necrotizing pancreatitis undergoing endoscopic transmural necrosectomy. Eligible participants were randomly assigned to case group (a novel strategy in which the stents were removed during the last necrosectomy when the necrosectomy endpoint was achieved) and control group (the conventional strategy in which the stents were removed after the last necrosectomy when clinical symptoms were relieved and fluid was nearly completely resolved confirmed by imaging). The primary endpoint was the incidence of composite complications within three months of enrollment.
Detailed Description
Over the last decade, approaches to managing necrotizing pancreatitis have evolved from open surgery to a minimally invasive approach due to the efficacy and lower morbidity and mortality rates of the latter technique. As one of minimally invasive approaches, endoscopic step-up approach, with transmural drainage whenever feasible and subsequent necrosectomy as required, was first described in 1996 and has evolved to first-line therapy for symptomatic necrotizing pancreatitis. However,The exact timing of transmural stent removal has not been well studied. The conventional strategy for stent removal in the published guidelines has been that patients should undergo follow-up imaging and stent removal at 4-8 weeks if walled-off necrosis has resolved. Here, we introduced a novel strategy in which the stents were removed during the last necrosectomy when the endpoint of endoscopic transmural necrosectomy was achieved, that was, the necrotic tissue was nearly completely removed, and the pink granulation tissue lining the wall was uncovered. Compared to the conventional strategy, the novel strategy avoided one endoscopy procedure. The present study is the first prospective, open-label, randomized controlled study to investigate the efficacy and safety of the novel strategy. We recruited and enrolled consecutive patients with necrotizing pancreatitis undergoing endoscopic transmural necrosectomy. Eligible participants were randomly assigned to case group (a novel strategy in which the stents were removed during the last necrosectomy when the necrosectomy endpoint was achieved) and control group (the conventional strategy in which the stents were removed after the last necrosectomy when clinical symptoms were relieved and fluid was nearly completely resolved confirmed by imaging). The primary endpoint was the incidence of composite complications within three months of enrollment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Pancreatitis, Necrotizing Pancreatitis, Walled-Off Necrosis
Keywords
Necrotizing pancreatitis, Endoscopic transmural necrosectomy, Lumen-apposing metal stent
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
156 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
The novel strategy group
Arm Type
Experimental
Arm Description
The stents were removed during the last necrosectomy when the endpoint of necrosectomy was achieved
Arm Title
The conventional strategy group
Arm Type
Active Comparator
Arm Description
The stent was removed after the last necrosectomy when clinical symptoms were relieved and fluid was nearly completely resolved confirmed by CT image
Intervention Type
Procedure
Intervention Name(s)
Stent removed by the novel strategy
Intervention Description
The stent was removed during the last necrosectomy when the endpoint of necrosectomy was achieved;
Intervention Type
Procedure
Intervention Name(s)
Stent removed by the conventional strategy
Intervention Description
The stent was removed after the last necrosectomy when clinical symptoms were relieved and fluid was nearly completely resolved confirmed by CT image.
Primary Outcome Measure Information:
Title
The incidence of composite complications
Description
The composite complications included new-onset organ failure or systemic complications、new-onset infectious pancreatic necrosis、abdominal or gastrointestinal bleeding, intestinal fistula, stent occlusion and stent migration.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
The incidence of technical success
Description
Technical success was defined by stent removed successfully.
Time Frame
3 months
Title
The incidence of clinical success
Description
Clinical success was defined as nearly completely resolution or <2 cm of collection assessed by image at the three-month follow-up without additional open surgery or death.
Time Frame
3 months
Title
The number of endoscopic transmural necrosectomy sessions
Description
Total sessions of patients undergoing endoscopic transmural necrosectomy.
Time Frame
3 months
Title
The number of additional endoscopic transmural necrosectomy sessions after stent removal
Description
Additional sessions of patients undergoing endoscopic transmural necrosectomy. after stent removal.
Time Frame
3 months
Title
Length of stent placement
Description
The duration time from stent placement to stent removal.
Time Frame
3 months
Title
The incidence of open surgery
Description
The incidence of patients needing open surgery after minimally invasive treatment.
Time Frame
3 months
Title
All-cause mortality
Description
The mortality whatever the cause is.
Time Frame
3 months
Title
Length of hospital stay
Description
The length of hospital stay due to necrotizing pancreatitis.
Time Frame
3 months
Title
The incidence of readmission
Description
The incidence of readmission after index discharge due to pancreatitis related problems.
Time Frame
12 months
Title
The hospital cost
Description
The hospital cost during hospitalization.
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients diagnosed with necrotizing pancreatitis according to the 2012 Atlanta classification criteria;
Patients aged between 18 and 65 years;
Patients who signed the informed consent;
Exclusion Criteria:
Patients without transmural stent placement;
Patients with transmural plastic stent not metal stent placement before enrollment;
Patients who underwent endoscopic transmural necrosectomy in other hospitals before admission;
Patients complicated with chronic pancreatitis;
Patients complicated with pancreatic tumor;
Pregnant or lactating women.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yin Zhu, PhD
Phone
86-791-88692507
Email
zhuyin27@sina.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yin Zhu, PhD
Organizational Affiliation
The First Affiliated Hospital of Nanchang University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The First Affiliated Hospital of Nanchang University
City
Nanchang
State/Province
Jiangxi
ZIP/Postal Code
330006
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yin Zhu, PhD
Phone
86-791-88692507
Email
zhuyin27@sina.com
12. IPD Sharing Statement
Learn more about this trial
Timing of Transmural Stent Removal in Necrotizing Pancreatitis
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